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4-二甲基氨基苯乙炔 | 17573-94-3

中文名称
4-二甲基氨基苯乙炔
中文别名
4-乙炔基-N,N-二甲基苯胺
英文名称
4-ethynyl-N,N-dimethylaniline
英文别名
4-dimethylaminophenylacetylene;4-(N,N-dimethylamino)phenylacetylene
4-二甲基氨基苯乙炔化学式
CAS
17573-94-3
化学式
C10H11N
mdl
——
分子量
145.204
InChiKey
ZWMAYLMVFSCMMS-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:
    49-53 °C (lit.)
  • 沸点:
    227.9±23.0 °C(Predicted)
  • 密度:
    0.98±0.1 g/cm3(Predicted)
  • 闪点:
    <110℃
  • 溶解度:
    可溶于DMSO(少许)、甲醇(少许)
  • 稳定性/保质期:
    按规定使用不会分解,避免接触氧化剂。

计算性质

  • 辛醇/水分配系数(LogP):
    2.7
  • 重原子数:
    11
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.2
  • 拓扑面积:
    3.2
  • 氢给体数:
    0
  • 氢受体数:
    1

安全信息

  • WGK Germany:
    3
  • 危险品标志:
    Xn
  • 安全说明:
    S26,S36
  • 危险标志:
    GHS07
  • 危险类别码:
    R36/37/38
  • 危险性描述:
    H315,H317,H319,H335
  • 危险性防范说明:
    P261,P280,P305 + P351 + P338
  • 海关编码:
    2921420090
  • 储存条件:
    请将药品存放在密闭、阴凉、干燥的地方。

SDS

SDS:c6cfe09488f100628d1f38432c61a3a0
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Section 1. IDENTIFICATION OF THE SUBSTANCE/MIXTURE
Product identifiers
Product name : 4-Ethynyl-N,N-dimethylaniline
CAS-No. : 17573-94-3


Section 2. HAZARDS IDENTIFICATION
Classification of the substance or mixture
Classification according to Regulation (EC) No 1272/2008 [EU-GHS/CLP]
Skin irritation (Category 2)
Eye irritation (Category 2)
Skin sensitization (Category 1)
Specific target organ toxicity - single exposure (Category 3)
Classification according to EU Directives 67/548/EEC or 1999/45/EC
Irritating to eyes, respiratory system and skin. May cause sensitization by inhalation and skin contact.
Label elements
Labelling according Regulation (EC) No 1272/2008 [CLP]
Pictogram
Signal word Warning
Hazard statement(s)
Causes skin irritation.
May cause an allergic skin reaction.
Causes serious eye irritation.
May cause respiratory irritation.
Precautionary statement(s)
Avoid breathing dust.
Wear protective gloves.
P305 + P351 + P338 IF IN EYES: Rinse cautiously with water for several minutes. Remove
contact lenses, if present and easy to do. Continue rinsing.
Supplemental Hazard none
Statements
According to European Directive 67/548/EEC as amended.
Hazard symbol(s)
R-phrase(s)
R36/37/38 Irritating to eyes, respiratory system and skin.
R42/43 May cause sensitization by inhalation and skin contact.
S-phrase(s)
S26 In case of contact with eyes, rinse immediately with plenty of water and
seek medical advice.
S36 Wear suitable protective clothing.
Other hazards - none

Section 3. COMPOSITION/INFORMATION ON INGREDIENTS
Substances
Synonyms : 1-Ethynyl-4-dimethylaniline
4-Dimethylaminophenylacetylene
Formula : C10H11N
Molecular Weight : 145,2 g/mol
Component Concentration
4-Ethynyl-N,N-dimethylaniline
CAS-No. 17573-94-3 -

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
Rinse thoroughly with plenty of water for at least 15 minutes and consult a physician.
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
To the best of our knowledge, the chemical, physical, and toxicological properties have not been
thoroughly investigated.
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
Carbon oxides, nitrogen oxides (NOx)
Advice for firefighters
Wear self contained breathing apparatus for fire fighting 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 vapors, mist or gas. Ensure
adequate ventilation. Evacuate personnel to safe areas. Avoid breathing dust.
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.Normal measures for preventive fire
protection.
Conditions for safe storage, including any incompatibilities
Store in cool place. Keep container tightly closed in a dry and well-ventilated place.
Specific end uses
no data available

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
Face shield and safety glasses 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).

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 Melting point/range: 49 - 53 °C - lit.
point
f) Initial boiling point and no data available
boiling range
g) Flash point < 110 °C - closed cup
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) Autoignition 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
no data available
Possibility of hazardous reactions
no data available
Conditions to avoid
no data available
Incompatible materials
Oxidizing agents
Hazardous decomposition products
Other decomposition products - no data available

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 sensitization
May cause allergic skin reaction.
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
Inhalation - May cause respiratory irritation.
Specific target organ toxicity - repeated exposure
no data available
Aspiration hazard
no data available
Potential health effects
Inhalation May be harmful if inhaled. Causes respiratory tract irritation.
Ingestion May be harmful if swallowed.
Skin May be harmful if absorbed through skin. Causes skin irritation.
Eyes Causes serious eye irritation.
Signs and Symptoms of Exposure
To the best of our knowledge, the chemical, physical, and toxicological properties have not been
thoroughly investigated.
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
no data available
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. Contact a licensed
professional waste disposal service to dispose of this material. 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


SECTION 16 - ADDITIONAL INFORMATION
N/A

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
    • 1
    • 2
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量
    • 1
    • 2
    • 3
    • 4
    • 5
    • 6

反应信息

  • 作为反应物:
    描述:
    4-二甲基氨基苯乙炔乙酸酐盐酸 作用下, 以 硝基甲烷 为溶剂, 20.0 ℃ 、101.33 kPa 条件下, 反应 4.0h, 以76%的产率得到p-dimethylamino-α-chlorostyrene
    参考文献:
    名称:
    末端芳烃与氯化氢的无催化剂氯化氢方案
    摘要:
    我们提出了一个简单直接的方案,用于在温和的反应条件下,使用氯化氢将末端芳基炔烃盐酸盐氯化为氯乙烯。该协议不涉及任何金属催化剂或添加剂。它简单,便宜且易于制备,并且显示出良好的反应活性。通过马尔可夫尼可夫加成规则,氢氯化作用进行得很顺利,从而产生独特的区域选择性产物。
    DOI:
    10.1016/j.cclet.2016.04.019
  • 作为产物:
    描述:
    N,N-二甲基苯胺 在 bis-triphenylphosphine-palladium(II) chloride 、 copper(l) iodide四丁基氟化铵过碘酸三乙胺 、 potassium iodide 作用下, 以 四氢呋喃二氯甲烷N,N-二甲基甲酰胺 为溶剂, 反应 3.0h, 生成 4-二甲基氨基苯乙炔
    参考文献:
    名称:
    钴催化的乙烯基氮丙啶的羰基化
    摘要:
    过渡金属催化的加氢炔基化反应是有效的转化反应,可直接形成官能化炔烃。其中,我们公开了乙烯基氮丙啶的钴催化的氢炔基化,其同时产生线性和支链的烯炔。反应条件的优化可以确定钴基催化体系的关键参数。范围研究表明,钴催化的氢化炔基化主要限于苯乙炔衍生物。在大多数情况下,以等摩尔比例分离出支链和线性烯炔(20例)。其他实验使我们可以提出一个合理的机制。最后,进一步使加氢烷基化产物进行碘环化,得到2,3-二氢吡咯衍生物和铂催化的环异构化。
    DOI:
    10.1002/adsc.202001575
  • 作为试剂:
    描述:
    C36H19N9O2S 在 4-二甲基氨基苯乙炔 作用下, 以 1,4-二氧六环 为溶剂, 以76%的产率得到C30H19N5O2S
    参考文献:
    名称:
    1,1,4,4-四甲基丁二烯官能化的蒽:合成的小近红外染料中的环加成物的区域选择性。
    摘要:
    通过仔细利用四氰基乙烯与蒽-酰胺衍生物的环加成反应的区域选择性,诱导了[2 + 2]或[4 + 2] Diels,获得了两个小的1,1,4,4-四氰基丁二烯官能化的发色团。 – Al火处理。DFT计算揭示了使用酰胺类化合物的[2 + 2]环加成-逆电环化反应序列的机理,并阐明了两种底物的不同机理。合成染料呈现全色吸收,并在高达1550 nm的固态下扩展到近红外和远红/近红外光致发光。
    DOI:
    10.1021/acs.orglett.1c00136
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文献信息

  • Application of Pd Nanoparticles Supported on Mesoporous Hollow Silica Nanospheres for the Efficient and Selective Semihydrogenation of Alkynes
    作者:Oscar Verho、Haoquan Zheng、Karl P. J. Gustafson、Anuja Nagendiran、Xiaodong Zou、Jan-E. Bäckvall
    DOI:10.1002/cctc.201501112
    日期:2016.2
    Herein, the preparation of a heterogeneous catalyst consisting of 1–2 nm sized Pd nanoparticles supported on amino‐functionalized mesoporous hollow silica nanospheres and its use for the semihydrogenation of mono‐ and disubstituted alkynes is reported. By utilizing this Pd nanocatalyst together with the green poisoning agent DMSO, high yields of the desired alkenes could be achieved, while suppressing
    在本文中,报道了由负载在氨基官能化介孔空心二氧化硅纳米球上的1-2 nm大小的Pd纳米颗粒组成的非均相催化剂的制备及其在单和双取代炔烃的半氢化反应中的应用。通过将此Pd纳米催化剂与绿色中毒剂DMSO一起使用,可以实现所需烯烃的高收率,同时抑制了烷烃过度还原的程度。令我们高兴的是,Pd纳米催化剂对炔烃部分表现出卓越的化学选择性,从而可以在其他可还原的官能团(例如卤素,羰基和硝基)存在下进行转化。
  • Discovery of Quinazolin-4(3<i>H</i>)-ones as NLRP3 Inflammasome Inhibitors: Computational Design, Metal-Free Synthesis, and in Vitro Biological Evaluation
    作者:Mohd Abdullaha、Shabber Mohammed、Mehboob Ali、Ajay Kumar、Ram A. Vishwakarma、Sandip B. Bharate
    DOI:10.1021/acs.joc.9b00138
    日期:2019.5.3
    NLRP3 inflammasome is an important therapeutic target for a number of human diseases. Herein, computationally designed series of quinazolin-4(3H)-ones were synthesized using iodine-catalyzed coupling of arylalkynes (or styrenes) with O-aminobenzamides. The key event in this transformation involves the oxidative cleavage of the C–C triple/double bond and the release of formaldehyde. The reaction relies
    NLRP3炎性小体是许多人类疾病的重要治疗靶标。本文中,使用碘催化的芳基炔烃(或苯乙烯)与O-氨基苯甲酰胺的偶联反应,合成了一系列计算设计的喹唑啉4(3 H)-1 。此转变的关键事件涉及C–C三键/双键的氧化裂解和甲醛的释放。该反应取决于在无金属条件下C–N键的形成以及C–C键的裂解。硝基取代的喹唑啉-4(3 H)-1 2k通过抑制从ATP刺激的J774A.1细胞中释放的IL-1β抑制NLRP3炎性小体(IC 50 5μM)。
  • COMPOSITIONS AND METHODS FOR DETECTING NERVE AGENTS
    申请人:Corcoran Robert C.
    公开号:US20100130757A1
    公开(公告)日:2010-05-27
    The present invention provides methods and compositions for detecting, identifying and measuring the abundance of chemical nerve agents. Methods and compositions of the present invention are capable of providing selective detection of phosphorous based nerve agents, such as nerve agents that are esters of methyl phosphonic acid derivatives incorporating a moderately good leaving group at the phosphorus. Selectivity in the present invention is provided by a sensor composition having an alpha (α) effect nucleophile group that undergoes specific nucleophilic substitution and rearrangement reactions with phosphorus based nerve agents having a tetrahederal phosphorous bound to oxygen. The present invention includes embodiments employing a sensor composition further comprising a reporter group covalently linked to the alpha effect nucleophile group allowing rapid optical readout of nerve agent detection events, including direct visual readout and optical readout via spectroscopic analysis.
    本发明提供了用于检测、识别和测量化学神经毒剂丰度的方法和组合物。本发明的方法和组合物能够选择性地检测基于磷的神经毒剂,例如酯化了在磷上具有中等良好离去基团的甲基膦酸衍生物的神经毒剂。本发明中的选择性是通过具有α效应亲核基团的传感器组合物提供的,该亲核基团与磷基神经毒剂发生特定的亲核取代和重排反应,其中磷与氧结合形成四面体磷。本发明包括采用传感器组合物的实施例,该传感器组合物进一步包括与α效应亲核基团共价连接的报告基团,允许对神经毒剂检测事件进行快速光学读数,包括直接视觉读数和通过光谱分析的光学读数。
  • 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。
  • LANTHANIDE CLUSTERS AND METHODS OF USE THEREOF
    申请人:YEDA RESEARCH AND DEVELOPMENT CO. LTD.
    公开号:US20160002269A1
    公开(公告)日:2016-01-07
    The present invention is directed to multinuclear lanthanides chiral clusters, based on phenyl-oxazoline-amide (POxA) ligands, and to methods of use thereof. The chiral clusters of this invention are highly fluorescent with high stability.
    本发明涉及基于苯基-噁唑啉酰胺(POxA)配体的多核镧系手性簇以及其使用方法。本发明的手性簇具有高荧光性能和高稳定性。
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(N-(2-甲基丙-2-烯-1-基)乙烷-1,2-二胺) (4-(苄氧基)-2-(哌啶-1-基)吡啶咪丁-5-基)硼酸 (11-巯基十一烷基)-,,-三甲基溴化铵 鼠立死 鹿花菌素 鲸蜡醇硫酸酯DEA盐 鲸蜡硬脂基二甲基氯化铵 鲸蜡基胺氢氟酸盐 鲸蜡基二甲胺盐酸盐 高苯丙氨醇 高箱鲀毒素 高氯酸5-(二甲氨基)-1-({(E)-[4-(二甲氨基)苯基]甲亚基}氨基)-2-甲基吡啶正离子 高氯酸2-氯-1-({(E)-[4-(二甲氨基)苯基]甲亚基}氨基)-6-甲基吡啶正离子 高氯酸2-(丙烯酰基氧基)-N,N,N-三甲基乙铵 马诺地尔 马来酸氢十八烷酯 马来酸噻吗洛尔EP杂质C 马来酸噻吗洛尔 马来酸倍他司汀 顺式环己烷-1,3-二胺盐酸盐 顺式氯化锆二乙腈 顺式吡咯烷-3,4-二醇盐酸盐 顺式双(3-甲氧基丙腈)二氯铂(II) 顺式3,4-二氟吡咯烷盐酸盐 顺式1-甲基环丙烷1,2-二腈 顺式-二氯-反式-二乙酸-氨-环己胺合铂 顺式-二抗坏血酸(外消旋-1,2-二氨基环己烷)铂(II)水合物 顺式-N,2-二甲基环己胺 顺式-4-甲氧基-环己胺盐酸盐 顺式-4-环己烯-1.2-二胺 顺式-4-氨基-2,2,2-三氟乙酸环己酯 顺式-2-甲基环己胺 顺式-2-(苯基氨基)环己醇 顺式-2-(氨基甲基)-1-苯基环丙烷羧酸盐酸盐 顺式-1,3-二氨基环戊烷 顺式-1,2-环戊烷二胺 顺式-1,2-环丁腈 顺式-1,2-双氨甲基环己烷 顺式--N,N'-二甲基-1,2-环己二胺 顺式-(R,S)-1,2-二氨基环己烷铂硫酸盐 顺式-(2-氨基-环戊基)-甲醇 顺-2-戊烯腈 顺-1,3-环己烷二胺 顺-1,3-双(氨甲基)环己烷 顺,顺-丙二腈 非那唑啉 靛酚钠盐 靛酚 霜霉威盐酸盐 霜脲氰