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1-(哌啶-1-基)丁烷-1,3-二酮 | 1128-87-6

中文名称
1-(哌啶-1-基)丁烷-1,3-二酮
中文别名
——
英文名称
1-(piperidin-1-yl)-butane-1,3-dione
英文别名
1-(piperidin-1-yl)-1,3-butanedione;1-(Piperidin-1-yl)butane-1,3-dione;1-piperidin-1-ylbutane-1,3-dione
1-(哌啶-1-基)丁烷-1,3-二酮化学式
CAS
1128-87-6
化学式
C9H15NO2
mdl
MFCD00090863
分子量
169.224
InChiKey
OVIHQCKYIOKFFX-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

  • 沸点:
    126-128 °C(Press: 4 Torr)
  • 密度:
    1.064±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    0.4
  • 重原子数:
    12
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.78
  • 拓扑面积:
    37.4
  • 氢给体数:
    0
  • 氢受体数:
    2

SDS

SDS:0214ae739da814798587bbf3b05f8bf2
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SECTION 1: Identification of the substance/mixture and of the company/undertaking
Product identifiers
Product name : N,N-Hexamethyleneacetoacetamide
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.
CAS-No. : 1128-87-6
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
Formula : C9H15NO2
Molecular weight : 169,23 g/mol
CAS-No. : 1128-87-6
Hazardous ingredients according to Regulation (EC) No 1272/2008
Component Classification Concentration
N,N-Hexamethyleneacetoacetamide
Acute Tox. 4; H302 <= 100 %
Hazardous ingredients according to Directive 1999/45/EC
Component Classification Concentration
N,N-Hexamethyleneacetoacetamide
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
No data available
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
No data available
Hazardous decomposition products
Other decomposition products - No data available
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

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
  • 下游产品
    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:
    1-(哌啶-1-基)丁烷-1,3-二酮 在 sodium azide 、 3-氯磺酰基苯甲酸potassium carbonate 、 potassium hydroxide 作用下, 以 乙腈 为溶剂, 反应 17.0h, 以56%的产率得到2-diazo-1-(piperidin-1-yl)ethanone
    参考文献:
    名称:
    通过重氮 C-C 键插入对富电子溴化苄衍生物进行同系化
    摘要:
    操纵 C-C 键进行选择性化学转化的能力具有挑战性,并且代表了一个不断增长的研究领域。在这里,我们报告了在简单的路易斯酸催化下,重氮化合物正式插入到苄基溴衍生物的“未活化”C-C键中。同系化反应通过苯鎓离子作为中间体进行,产物含有苄型季铵中心和适合进一步衍生化的烷基溴。计算分析提供了对反应机制的重要见解,特别是关键的选择性决定步骤。
    DOI:
    10.1021/jacs.1c11503
  • 作为产物:
    描述:
    2-Chloro-1-(piperidin-1-yl)butane-1,3-dionepotassium carbonate4-甲苯硫酚 作用下, 以 乙腈 为溶剂, 反应 1.5h, 以100%的产率得到1-(哌啶-1-基)丁烷-1,3-二酮
    参考文献:
    名称:
    在 K+/CH3CN 体系中使用苯硫醇对 α-卤代羰基化合物进行还原脱卤的简便方法
    摘要:
    图形摘要 摘要 苯硫醇作为各种 α-卤代羰基化合物脱卤的还原剂,在 K+/CH3CN 系统中进行了研究。该反应在温和的反应条件下以高产率提供还原的化合物,尤其是 α-氯代羰基化合物。此外,在超声波照射下进行的反应大大缩短了反应时间。
    DOI:
    10.1080/10426507.2016.1138309
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文献信息

  • Efficient Water Reduction with sp<sup>3</sup> -sp<sup>3</sup> Diboron(4) Compounds: Application to Hydrogenations, H-D Exchange Reactions, and Carbonyl Reductions
    作者:Mathias Flinker、Hongfei Yin、René W. Juhl、Espen Z. Eikeland、Jacob Overgaard、Dennis U. Nielsen、Troels Skrydstrup
    DOI:10.1002/anie.201709685
    日期:2017.12.11
    demonstrated by conducting a series of selective reductions of alkynes and alkenes, and hydrogen–deuterium exchange reactions using two‐chamber reactors. Finally, as the water reduction reaction generates an intermediate borohydride species, a range of aldehydes and ketones were reduced by using water as the hydride source.
    合成了一系列结晶的sp 3 -sp 3 diboron(4)化合物,它们显示出促进形成二氢的水的简便还原。通过对乙炔和烯烃进行一系列的选择性还原,以及使用两室反应器进行氢-氘交换反应,证明了这些二硼作为简单有效的二氢和二氘源的应用。最后,由于水还原反应生成了中间的硼氢化物,通过使用水作为氢化物源,可以还原一系列醛和酮。
  • One Pot Synthesis of Micromolar BACE-1 Inhibitors Based on the Dihydropyrimidinone Scaffold and Their Thia and Imino Analogues
    作者:Jessica Bais、Fabio Benedetti、Federico Berti、Iole Cerminara、Sara Drioli、Maria Funicello、Giorgia Regini、Mattia Vidali、Fulvia Felluga
    DOI:10.3390/molecules25184152
    日期:——

    A library of dihydropyrimidinones was synthesized via a “one-pot” three component Biginelli reaction using different aldehydes in combination with β-dicarbonyl compounds and urea. Selected 2-thiooxo and 2-imino analogs were also obtained with the Biginelli reaction from thiourea and guanidine hydrochloride, respectively. The products were screened in vitro for their β-secretase inhibitory activity. The majority of the compounds resulted to be active, with IC50 in the range 100 nM–50 μM.

    通过使用不同的醛与β-二羰基化合物和尿素的“一锅法”三组分Biginelli反应合成了一系列二氢嘧啶酮类化合物。选择性地,也从硫脲和盐酸胍得到了2-硫氧代和2-亚氨基类似物。这些产物在体外被筛选,用于评估它们的β-分泌酶抑制活性。大多数化合物表现出活性,IC50在100 nM至50 μM范围内。
  • Fe(III) Complex Compounds For The Treatment And Prophylaxis Of Iron Deficiency Symptoms And Iron Deficiency Anemias
    申请人:Bark Thomas
    公开号:US20130109662A1
    公开(公告)日:2013-05-02
    The invention relates to iron(III) complex compounds and pharmaceutical compositions comprising them for the use as medicaments, in particular for the treatment and/or prophylaxis of iron deficiency symptoms and iron deficiency anemias.
    这项发明涉及铁(III)配合物和包括它们的药物组合物,用作药物,特别是用于治疗和/或预防缺铁症状和缺铁性贫血。
  • Rh(III)-Catalyzed Redox-Neutral Annulation of Primary Benzamides with Diazo Compounds: Approach to Isoquinolinones
    作者:Youzhi Wu、Peng Sun、Kaifan Zhang、Tie Yang、Hequan Yao、Aijun Lin
    DOI:10.1021/acs.joc.5b02824
    日期:2016.3.4
    Reported herein is a Rh-catalyzed redox-neutral annulation of primary benzamides with diazo compounds, representing an efficient and economic protocol to isoquinolinones. The procedure exhibited good functional group tolerability, scalability, and regioselectivity, obviating the need for oxidants, and only environmentally benign N2 and H2O were released. Further utilization of the method provided an
    本文报道的是初级苯甲酰胺与重氮化合物的Rh催化氧化还原中性环化反应,代表了对异喹啉酮的有效和经济方案。该过程表现出良好的官能团耐受性,可伸缩性,和区域选择性,避免了对氧化剂的需要,并且只对环境无害Ñ 2和H 2 ö被释放。该方法的进一步利用为功能化的异喹啉提供了另一种途径。
  • COMPOSITIONS COMPRISING A POLYMERIC NETWORK
    申请人:UNIVERSITEIT GENT
    公开号:US20170327625A1
    公开(公告)日:2017-11-16
    The present invention relates to a composition comprising a polymeric network having at least one unit of formula (I), (II), and/or (III); (I) (II) (III) wherein said composition is obtained by contacting at least one compound A comprising at least two functions selected from the group of function of formula X—C(═O)—CHR 1 —C(═O)—R 2 , —C(═O)—C—R 2 ; or —C(═O)—CR 1 ═CR 2 —NR 4 R 5 ; wherein at least 25% by weight of compounds A have a functionality ≦5, with % by weight relative to the total weight of compounds A; with at least one compound B comprising at least one NH 2 , or NH 3 + groups; wherein X, R 1 , R 2 , R 3 , R 4 , R 5 , L 1 and L 2 have the same meaning as that defined in the claims. The present invention also relates to a compound comprising at least two units and at most 5 units of formula (I), (II), and/or (III); wherein R 1 , R 2 , R 3 , X, L 1 and L 2 have the same meaning as that defined in the claims. The present invention also relates to processes for preparing said composition and said compounds, to material, articles, and polymers comprising or using said compositions and compounds, and the use thereof.
    本发明涉及一种组合物,其包括至少一种具有式(I)、(II)和/或(III)的聚合网络单元;其中所述组合物是通过接触至少一种化合物A而获得的,所述化合物A包括至少两种选自以下功能组的功能:X—C(═O)—CHR1—C(═O)—R2,—C(═O)—C—R2;或—C(═O)—CR1═CR2—NR4R5;其中化合物A的至少25%的重量具有功能性≦5,以重量百分比相对于化合物A的总重量计算;以及至少一种包括至少一个NH2或NH3+基团的化合物B;其中X、R1、R2、R3、R4、R5、L1和L2的含义与权利要求书中定义的含义相同。本发明还涉及一种化合物,其包括至少两个单元和最多5个式(I)、(II)和/或(III)的单元;其中R1、R2、R3、X、L1和L2的含义与权利要求书中定义的含义相同。本发明还涉及制备所述组合物和所述化合物的方法,以及包括或使用所述组合物和化合物的材料、物品和聚合物,以及其用途。
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