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3-甲基-3-羧基-1-氧杂环丁烷 | 28562-68-7

中文名称
3-甲基-3-羧基-1-氧杂环丁烷
中文别名
3-甲基-3-氧杂环丁烷羧酸;3-甲基噁丁环甲酸
英文名称
3-methyloxetane-3-carboxylic acid
英文别名
3-methyl-3-oxetanecarboxylic acid
3-甲基-3-羧基-1-氧杂环丁烷化学式
CAS
28562-68-7
化学式
C5H8O3
mdl
MFCD09842435
分子量
116.117
InChiKey
PMPZEEUNGQSAIQ-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

物化性质

  • 熔点:
    58-60℃
  • 沸点:
    224℃
  • 密度:
    1.252
  • 闪点:
    99℃

计算性质

  • 辛醇/水分配系数(LogP):
    -0.3
  • 重原子数:
    8
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.8
  • 拓扑面积:
    46.5
  • 氢给体数:
    1
  • 氢受体数:
    3

安全信息

  • 危险等级:
    IRRITANT
  • 海关编码:
    2932999099
  • WGK Germany:
    3
  • 危险标志:
    GHS07
  • 危险性描述:
    H302
  • 危险性防范说明:
    P261,P305+P351+P338
  • 储存条件:
    温度范围:0-10°C;请勿加热。

SDS

SDS:120eb17e9ad92e0d7bf9aeede454a70f
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SECTION 1: Identification of the substance/mixture and of the company/undertaking
Product identifiers
Product name : 3-Methyloxetane-3-Carboxylic Acid
REACH No. : A registration number is not available for this substance as the substance
or its uses are exempted from registration, the annual tonnage does not
require a registration or the registration is envisaged for a later
registration deadline.
Relevant identified uses of the substance or mixture and uses advised against
Identified uses : Laboratory chemicals, Manufacture of substances



SECTION 2: Hazards identification
Classification of the substance or mixture
Classification according to Regulation (EC) No 1272/2008
Acute toxicity, Oral (Category 4), H302
For the full text of the H-Statements mentioned in this Section, see Section 16.
Classification according to EU Directives 67/548/EEC or 1999/45/EC
Xn Harmful R22
For the full text of the R-phrases mentioned in this Section, see Section 16.
Label elements
Labelling according Regulation (EC) No 1272/2008
Pictogram
Signal word Warning
Hazard statement(s)
H302 Harmful if swallowed.
Precautionary statement(s) none
Supplemental Hazard none
Statements
Other hazards
This substance/mixture contains no components considered to be either persistent, bioaccumulative and
toxic (PBT), or very persistent and very bioaccumulative (vPvB) at levels of 0.1% or higher.

SECTION 3: Composition/information on ingredients
Substances
Molecular weight : 116,12 g/mol
Hazardous ingredients according to Regulation (EC) No 1272/2008
Component Classification Concentration
3-Methyloxetane-3-Carboxylic Acid
Acute Tox. 4; H302 <= 100 %
Hazardous ingredients according to Directive 1999/45/EC
Component Classification Concentration
3-Methyloxetane-3-Carboxylic Acid
Xn, R22 <= 100 %
For the full text of the H-Statements and R-Phrases mentioned in this Section, see Section 16

SECTION 4: First aid measures
Description of first aid measures
General advice
Consult a physician. Show this safety data sheet to the doctor in attendance.
If inhaled
If breathed in, move person into fresh air. If not breathing, give artificial respiration. Consult a physician.
In case of skin contact
Wash off with soap and plenty of water. Consult a physician.
In case of eye contact
Flush eyes with water as a precaution.
If swallowed
Never give anything by mouth to an unconscious person. Rinse mouth with water. Consult a physician.
Most important symptoms and effects, both acute and delayed
The most important known symptoms and effects are described in the labelling (see section 2.2) and/or in
section 11
Indication of any immediate medical attention and special treatment needed
No data available

SECTION 5: Firefighting measures
Extinguishing media
Suitable extinguishing media
Use water spray, alcohol-resistant foam, dry chemical or carbon dioxide.
Special hazards arising from the substance or mixture
Nature of decomposition products not known.
Advice for firefighters
Wear self-contained breathing apparatus for firefighting if necessary.
Further information
No data available

SECTION 6: Accidental release measures
Personal precautions, protective equipment and emergency procedures
Use personal protective equipment. Avoid dust formation. Avoid breathing vapours, mist or gas. Ensure
adequate ventilation. Avoid breathing dust.
For personal protection see section 8.
Environmental precautions
Do not let product enter drains.
Methods and materials for containment and cleaning up
Pick up and arrange disposal without creating dust. Sweep up and shovel. Keep in suitable, closed
containers for disposal.
Reference to other sections
For disposal see section 13.

SECTION 7: Handling and storage
Precautions for safe handling
Avoid contact with skin and eyes. Avoid formation of dust and aerosols.
Provide appropriate exhaust ventilation at places where dust is formed.
For precautions see section 2.2.
Conditions for safe storage, including any incompatibilities
Store in cool place. Keep container tightly closed in a dry and well-ventilated place.
Storage class (TRGS 510): Non Combustible Solids
Specific end use(s)
Apart from the uses mentioned in section 1.2 no other specific uses are stipulated

SECTION 8: Exposure controls/personal protection
Control parameters
Components with workplace control parameters
Exposure controls
Appropriate engineering controls
Handle in accordance with good industrial hygiene and safety practice. Wash hands before breaks and
at the end of workday.
Personal protective equipment
Eye/face protection
Safety glasses with side-shields conforming to EN166 Use equipment for eye protection tested
and approved under appropriate government standards such as NIOSH (US) or EN 166(EU).
Skin protection
Handle with gloves. Gloves must be inspected prior to use. Use proper glove removal technique
(without touching glove's outer surface) to avoid skin contact with this product. Dispose of
contaminated gloves after use in accordance with applicable laws and good laboratory practices.
Wash and dry hands.
The selected protective gloves have to satisfy the specifications of EU Directive 89/686/EEC and
the standard EN 374 derived from it.
Body Protection
Complete suit protecting against chemicals, The type of protective equipment must be selected
according to the concentration and amount of the dangerous substance at the specific workplace.
Respiratory protection
For nuisance exposures use type P95 (US) or type P1 (EU EN 143) particle respirator.For higher
level protection use type OV/AG/P99 (US) or type ABEK-P2 (EU EN 143) respirator cartridges.
Use respirators and components tested and approved under appropriate government standards
such as NIOSH (US) or CEN (EU).
Control of environmental exposure
Do not let product enter drains.

SECTION 9: Physical and chemical properties
Information on basic physical and chemical properties
a) Appearance Form: solid
b) Odour No data available
c) Odour Threshold No data available
d) pH No data available
e) Melting point/freezing No data available
point
f) Initial boiling point and No data available
boiling range
g) Flash point No data available
h) Evaporation rate No data available
i) Flammability (solid, gas) No data available
j) Upper/lower No data available
flammability or
explosive limits
k) Vapour pressure No data available
l) Vapour density No data available
m) Relative density No data available
n) Water solubility No data available
o) Partition coefficient: n- No data available
octanol/water
p) Auto-ignition No data available
temperature
q) Decomposition No data available
temperature
r) Viscosity No data available
s) Explosive properties No data available
t) Oxidizing properties No data available
Other safety information
No data available

SECTION 10: Stability and reactivity
Reactivity
No data available
Chemical stability
Stable under recommended storage conditions.
Possibility of hazardous reactions
No data available
Conditions to avoid
No data available
Incompatible materials
Strong oxidizing agents
Hazardous decomposition products
In the event of fire: see section 5

SECTION 11: Toxicological information
Information on toxicological effects
Acute toxicity
No data available
Skin corrosion/irritation
No data available
Serious eye damage/eye irritation
No data available
Respiratory or skin sensitisation
No data available
Germ cell mutagenicity
No data available
Carcinogenicity
IARC: No component of this product present at levels greater than or equal to 0.1% is identified as
probable, possible or confirmed human carcinogen by IARC.
Reproductive toxicity
No data available
Specific target organ toxicity - single exposure
No data available
Specific target organ toxicity - repeated exposure
No data available
Aspiration hazard
No data available
Additional Information
RTECS: Not available
To the best of our knowledge, the chemical, physical, and toxicological properties have not been
thoroughly investigated.

SECTION 12: Ecological information
Toxicity
No data available
Persistence and degradability
No data available
Bioaccumulative potential
No data available
Mobility in soil
No data available
Results of PBT and vPvB assessment
This substance/mixture contains no components considered to be either persistent, bioaccumulative and
toxic (PBT), or very persistent and very bioaccumulative (vPvB) at levels of 0.1% or higher.
Other adverse effects
No data available

SECTION 13: Disposal considerations
Waste treatment methods
Product
Offer surplus and non-recyclable solutions to a licensed disposal company. Dissolve or mix the material
with a combustible solvent and burn in a chemical incinerator equipped with an afterburner and scrubber.
Contaminated packaging
Dispose of as unused product.

SECTION 14: Transport information
UN number
ADR/RID: - IMDG: - IATA: -
UN proper shipping name
ADR/RID: Not dangerous goods
IMDG: Not dangerous goods
IATA: Not dangerous goods
Transport hazard class(es)
ADR/RID: - IMDG: - IATA: -
Packaging group
ADR/RID: - IMDG: - IATA: -
Environmental hazards
ADR/RID: no IMDG Marine pollutant: no IATA: no
Special precautions for user
No data available

SECTION 15: Regulatory information
This safety datasheet complies with the requirements of Regulation (EC) No. 1907/2006.
Safety, health and environmental regulations/legislation specific for the substance or mixture
No data available
Chemical Safety Assessment
For this product a chemical safety assessment was not carried out

SECTION 16: Other information
Full text of H-Statements referred to under sections 2 and 3.
Acute Tox. Acute toxicity
H302 Harmful if swallowed.
Full text of R-phrases referred to under sections 2 and 3
Xn Harmful
R22 Harmful if swallowed.
Further information
Copyright 2014 Co. LLC. License granted to make unlimited paper copies for internal use
only.
The above information is believed to be correct but does not purport to be all inclusive and shall be
used only as a guide. The information in this document is based on the present state of our knowledge
and is applicable to the product with regard to appropriate safety precautions. It does not represent any
guarantee of the properties of the product. Corporation and its Affiliates shall not be held
liable for any damage resulting from handling or from contact with the above product. See
and/or the reverse side of invoice or packing slip for additional terms and conditions of sale.

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    3-甲基-3-羧基-1-氧杂环丁烷正丁基锂N,N-二异丙基乙胺 、 N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate 作用下, 以 四氢呋喃正己烷N,N-二甲基甲酰胺 为溶剂, 反应 13.75h, 生成 1-(4-methoxyphenyl)-1-(3-methyloxetan-3-yl)prop-2-en-1-ol
    参考文献:
    名称:
    通过质子耦合电子转移实现烯丙醇中的 1,3-烷基转位
    摘要:
    描述了一种通过 1,3-烷基转位将无环烯丙醇异构化为 β-官能化酮的方法。该反应通过光驱动的质子耦合电子转移 (PCET) 激活烯丙醇底物中的 O-H 键,随后产生的烷氧基自由基的 C-C β-断裂来进行。在断裂事件中产生的瞬态烷基自由基和烯酮受体随后通过自由基共轭加成重组以提供 β-官能化酮产物。多种带有烷基和酰基迁移基团的烯丙醇底物被成功地调节。来自机理研究的见解导致改进的反应方案提高了对具有挑战性的底物的反应性能。
    DOI:
    10.1002/anie.202105285
  • 作为产物:
    描述:
    3-甲基-3-羟甲基氧杂环丁烷2,2,6,6-四甲基哌啶氧化物 、 sodium bromide 、 sodium hydroxide 、 sodium hypochlorite 作用下, 以 1,2-二氯乙烷丙酮 为溶剂, 生成 3-甲基-3-羧基-1-氧杂环丁烷
    参考文献:
    名称:
    自动机器学习辅助 TEMPO 催化伯醇氧化制备羧酸
    摘要:
    尽管醇氧化被认为是成熟的反应,但选择生产条件或预测未见醇的反应产率仍然是主要挑战。在此,公开了一种用于将伯醇催化氧化为相应羧酸的自动机器学习 (ML) 模型。使用高通量实验 (HTE) 生成了包含 3444 个数据的数据集,其中包含 282 种伯醇和 45 种条件。使用 HTE 数据和 105 个描述符,使用 AutoGluon(开源自动机器学习框架)和 KNIME(开源数据分析平台)执行多标签预测。对于 240 次反应的独立测试(20 种未见醇和 12 种条件的完整矩阵),AutoGluon 和用于产量预测的多标签预测 (AGMP) 表现出色。R 2为0.767,MAE为4.9%。该模型还表明,新生成的描述符(Y/N,反应反应性分类)是与产量预测最相关的描述符,为将 HTE 和 ML 集成到有机合成中提供了新的视角。
    DOI:
    10.1002/cjoc.202200555
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文献信息

  • [EN] PYRIMIDINE COMPOUNDS, COMPOSITIONS AND METHODS OF USE<br/>[FR] COMPOSÉS DE PYRIMIDINE, COMPOSITIONS ET PROCÉDÉS D'UTILISATION
    申请人:GENENTECH INC
    公开号:WO2010014939A1
    公开(公告)日:2010-02-04
    Disclosed are compounds of Formula I, including steroisomers, geometric isomers, tautomers, solvates, metabolites and pharmaceutically acceptable salts thereof, that are useful in modulating PIKK related kinase signaling, e.g., mTOR, and for the treatment of diseases (e.g., cancer) that are mediated at least in part by the dysregulation of the PIKK signaling pathway (e.g., mTOR).
    揭示了公式I的化合物,包括立体异构体、几何异构体、互变异构体、溶剂合物、代谢物和其药学上可接受的盐,这些化合物在调节PIKK相关激酶信号传导方面很有用,例如mTOR,并用于治疗至少部分由PIKK信号传导途径失调引起的疾病(例如癌症)。
  • Nickel-catalyzed site- and stereoselective reductive alkylalkynylation of alkynes
    作者:Yi Jiang、Jiaoting Pan、Tao Yang、Yu Zhao、Ming Joo Koh
    DOI:10.1016/j.chempr.2020.12.024
    日期:2021.4
    that the synthesis of stereodefined 1,3-enynes featuring a trisubstituted olefin is achieved by merging alkynes, alkynyl bromides, and redox-active N-(acyloxy)phthalimides through nickel-catalyzed reductive alkylalkynylation. Products are generated in up to an 89% yield as single regio- and E isomers. Transformations are tolerant of diverse functional groups and the resulting 1,3-enynes are amenable
    通过正交活化容易获得的底物进行炔烃的流线型双官能化开发催化多组分反应是有机化学中一个引人注目的目标。尤其是炔烃羰基化可以直接进入具有不同取代模式的有价值的1,3-烯炔。在这里,我们显示了通过合并炔烃,炔基溴化物和氧化还原活性的N-(酰氧基)邻苯二甲酰亚胺,通过镍催化的还原性烷基炔基化反应,可以合成具有三取代烯烃的立体定义的1,3-烯炔。单一区域和E生成的产品产率高达89%异构体。转化耐受各种官能团,并且所得的1,3-烯炔适合进一步加工成合成上有用的结构单元。利用烯烃系的N-(酰氧基)邻苯二甲酰亚胺,可以实施级联自由基加成/环化/炔基化方法以获得1,5-烯炔。这项研究强调了氧化还原活性酯与卤代烷烃相比在还原性炔烃双碳官能化中作为优越的烷基供体的关键作用。
  • Organocatalytic decarboxylative alkylation of <i>N</i>-hydroxy-phthalimide esters enabled by pyridine-boryl radicals
    作者:Liuzhou Gao、Guoqiang Wang、Jia Cao、Dandan Yuan、Cheng Xu、Xuewen Guo、Shuhua Li
    DOI:10.1039/c8cc06152a
    日期:——
    The decarboxylative alkylation of N-hydroxyphthalimide (NHPI) based reactive esters with olefins has been achieved via an organocatalytic strategy. Control experiments and density functional theory calculations suggest that these reactions involve a boryl-radical mediated decarboxylation pathway, which is different from the single electron transfer involved in decarboxylative alkylation reactions reported
    N-羟基邻苯二甲酰亚胺(NHPI)基反应性酯与烯烃的脱羧烷基化已通过有机催化策略实现。对照实验和密度泛函理论计算表明,这些反应涉及硼基自由基介导的脱羧途径,该途径不同于先前报道的脱羧烷基化反应中涉及的单电子转移。这种无金属的脱羧烷基化反应具有良好的功能相容性,并且通过烷基和芳基羧酸衍生物的转化说明了广泛的底物范围。
  • Decarboxylative Amination: Diazirines as Single and Double Electrophilic Nitrogen Transfer Reagents
    作者:Preeti P. Chandrachud、Lukasz Wojtas、Justin M. Lopchuk
    DOI:10.1021/jacs.0c09403
    日期:2020.12.30
    structure and functionality of the substrate to be aminated. Further, many of these reagents are challenging to handle, engage in undesired side reactions, and function only within a narrow scope. Here we report the use of diazirines as practical reagents for the decarboxylative amination of simple and complex redox-active esters. The diaziridines thus produced are readily diversifiable to amines, hydrazines
    含氮小分子在医学中无处不在,需要继续寻找改进的 CN 键形成方法。亲电胺化通常需要不同的试剂工具包,其选择取决于待胺化底物的特定结构和功能。此外,这些试剂中的许多都难以处理,会发生不需要的副反应,并且只能在狭窄的范围内发挥作用。在这里,我们报告了使用 diazirines 作为简单和复杂的氧化还原活性酯脱羧胺化的实用试剂。由此产生的二氮丙啶很容易在一个步骤中多样化为胺、肼和含氮杂环。该反应也已应用于全氟化二氮嗪的氟相合成。
  • Photodecarboxylative Amination of Redox-Active Esters with Diazirines
    作者:Vishala Maharaj、Preeti P. Chandrachud、Wen Che、Lukasz Wojtas、Justin M. Lopchuk
    DOI:10.1021/acs.orglett.1c03344
    日期:2021.11.19
    Diazirines have been recently demonstrated to serve as electrophilic amination reagents that afford diaziridines, versatile heterocycles that are readily transformed into amines, hydrazines, and nitrogen-containing heterocycles. Here, we report the photodecarboxylative amination of redox-active esters with diazirines using inexpensive photoactivators under mild conditions with an enhanced scope for
    最近已证明二氮丙啶可用作亲电胺化试剂,可提供二氮丙啶、多种杂环,这些杂环很容易转化为胺、肼和含氮杂环。在这里,我们报告了在温和条件下使用廉价的光活化剂对氧化还原活性酯与二氮丙啶进行光脱羧胺化,并扩大了主要底物的范围。证明了二氮丙啶对蓝光的稳定性,为进一步研究具有这些独特杂环的其他光化学胺化方法铺平了道路。
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同类化合物

顺-2,4-二甲基氧杂环丁烷 硫酰胺,N-[4-(氰基甲基)苯基]- 甲基(噁丁环烷-3-基甲基)胺 氧杂环丁烷-3-胺盐酸盐 氧杂环丁烷-3-硫醇 氧杂环丁烷-3-甲醛 氧杂环丁烷-3-甲醇 氧杂环丁烷-3-乙酸乙酯 氧杂环丁烷-2-甲酸乙酯 氧杂环丁-3-醇 噁丁环,3-[[(10-溴癸基)氧代]甲基]-3-甲基- 反-2,4-二甲基氧杂环丁烷 乙基-3-丙基-2-氧杂环丁烷 乙基-2-氧杂环丁烷 三甲氧基酯 三甲基((3-甲基氧杂环丁烷-3-基)乙炔)硅烷 [3-(甲基氨基)氧杂环丁-3-基]甲醇 O-(氧杂环丁烷-3-基)羟胺 N,3-二甲基-3-氧杂环丁烷甲胺 7-氧杂二环[4.2.0]辛烷 6-碘-2-氧杂螺[3.3]庚烷 6-噁-1-氮杂螺[3.3]庚烷草酸盐 5-氟-3,3-二甲基-1-氧杂螺[3.5]壬烷 4,4-二甲基-2-氧杂环丁烷甲腈 3-胺乙基氧杂环丁烷 3-羟乙基氧杂环丁烷 3-碘甲基-3-甲基氧杂环丁烷 3-碘氧杂环丁烷 3-硝基亚甲基-氧杂环丁烷 3-硝基-1-氧杂环丁烷 3-甲氨基氧杂环丁烷 3-甲氧基氧杂环丁烷 3-甲基环氧丁烷 3-甲基氧杂-3-胺盐酸盐 3-甲基-3-醛基-1-氧杂环丁烷 3-甲基-3-胺甲基-1-氧杂环丁烷 3-甲基-3-羧基-1-氧杂环丁烷 3-甲基-3-羟甲基氧杂环丁烷 3-甲基-3-氧杂环丁烷乙酸 3-甲基-3-[(2,2,2-三氟乙氧基)甲基]氧杂环丁烷 3-甲基-3-(2,2,3,3,3-五氟丙氧基)氧杂环丁烷 3-甲基 3-氨基氧杂环丁烷 3-环己基氧杂环丁烷 3-溴甲基-3-羟甲基-1-氧杂环丁烷 3-溴甲基-3-甲基-1-氧杂环丁烷 3-溴甲基-3-氯甲基-1-氧杂环丁烷 3-溴甲基-3-氟氧杂环丁烷 3-溴环氧丁烷 3-氯甲基-3-碘甲基-1-氧杂环丁烷 3-氯氧杂环丁烷