2-氯-1-(4-乙基苯基)-乙酮 | 50690-09-0

• 分子结构分类: 有机化合物 - 有机氧化合物
• 中文名称: 2-氯-1-(4-乙基苯基)-乙酮
• 中文别名: 2-氯-1-(4-乙基苯基)乙酮
• 英文名称: 2-chloro-1-(4-ethylphenyl)ethan-1-one
• 英文别名: 2-Chloro-1-(4-ethylphenyl)ethanone
• CAS: 50690-09-0
• 化学式: C₁₀H₁₁ClO
• mdl: MFCD03964194
• 分子量: 182.65
• InChiKey: MLDROUSGWZPVMD-UHFFFAOYSA-N

物化性质

• 熔点：
  38-39 °C
• 沸点：
  147-150 °C(Press: 10 Torr)
• 密度：
  1.105±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  3
• 重原子数：
  12
• 可旋转键数：
  3
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.3
• 拓扑面积：
  17.1
• 氢给体数：
  0
• 氢受体数：
  1

安全信息

• 海关编码：
  2914700090

SDS

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SECTION 1: Identification of the substance/mixture and of the company/undertaking
Product identifiers
Product name : 2-Chloro-1-(4-Ethylphenyl)Ethanone
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

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SECTION 2: Hazards identification
Classification of the substance or mixture
Not a hazardous substance or mixture according to Regulation (EC) No. 1272/2008.
This substance is not classified as dangerous according to Directive 67/548/EEC.
Label elements
The product does not need to be labelled in accordance with EC directives or respective national laws.
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.

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SECTION 3: Composition/information on ingredients
Substances
Molecular weight : 182,65 g/mol
No components need to be disclosed according to the applicable regulations.

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SECTION 4: First aid measures
Description of first aid measures
If inhaled
If breathed in, move person into fresh air. If not breathing, give artificial respiration.
In case of skin contact
Wash off with soap and plenty of water.
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.
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

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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

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SECTION 6: Accidental release measures
Personal precautions, protective equipment and emergency procedures
Avoid dust formation. Avoid breathing vapours, mist or gas.
For personal protection see section 8.
Environmental precautions
No special environmental precautions required.
Methods and materials for containment and cleaning up
Sweep up and shovel. Keep in suitable, closed containers for disposal.
Reference to other sections
For disposal see section 13.

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SECTION 7: Handling and storage
Precautions for safe handling
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

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SECTION 8: Exposure controls/personal protection
Control parameters
Components with workplace control parameters
Exposure controls
Appropriate engineering controls
General industrial hygiene practice.
Personal protective equipment
Eye/face protection
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
Choose body protection in relation to its type, to the concentration and amount of dangerous
substances, and to the specific work-place., The type of protective equipment must be selected
according to the concentration and amount of the dangerous substance at the specific workplace.
Respiratory protection
Respiratory protection is not required. Where protection from nuisance levels of dusts are desired,
use type N95 (US) or type P1 (EN 143) dust masks. Use respirators and components tested and
approved under appropriate government standards such as NIOSH (US) or CEN (EU).
Control of environmental exposure
No special environmental precautions required.

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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

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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
In the event of fire: see section 5

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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

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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

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SECTION 13: Disposal considerations
Waste treatment methods
Product
Offer surplus and non-recyclable solutions to a licensed disposal company.
Contaminated packaging
Dispose of as unused product.

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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

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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

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SECTION 16: Other information
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.

反应信息

• 作为反应物：
  描述：

  2-氯-1-(4-乙基苯基)-乙酮 在 copper(l) iodide 、 samarium (III) iodide 、 N,N-二甲基甲酰胺 作用下， 反应 2.0h， 以72%的产率得到
  参考文献：
  名称：

  SmI 3 / CuI †促进的α-卤代酮的新型偶联反应

  摘要：

  以SmI 3作为路易斯酸并在DMF中被CuI催化，α-卤代酯意外地转化为α-羟基-1,4-二酮，产率中等至中等。探讨了该机制，并提出了合理的反应途径。假定DMF既起着羟基源的作用又起着溶剂的双重作用。

  DOI：

  10.1039/c5ra26604a
• 作为产物：
  描述：

  4-乙基苯乙炔 在 甲醇 、 gold(III) chloride 、 双三氟甲烷磺酰亚胺银盐 、 N-氯代丁二酰亚胺 作用下， 以 1,4-二氧六环 为溶剂， 以85%的产率得到2-氯-1-(4-乙基苯基)-乙酮
  参考文献：
  名称：

  AuIII催化从末端炔烃形成α-卤代甲基酮

  摘要：

  开发了一种 AuIII 催化的从末端炔烃合成 α-卤代甲基酮的方法。这种方法对芳香族和脂肪族末端炔烃具有优异的官能团兼容性和良好的产率。所得的α-卤代甲基酮用于制备杂环茚茚结构。提出了一锅反应的合理机制。

  DOI：

  10.1002/ejoc.201601416

文献信息

• Metal-free hydration of aromatic haloalkynes to α-halomethyl ketones
  作者：Min Ye、Yuelu Wen、Huifang Li、Yejuan Fu、Qinghao Wang

  DOI：10.1016/j.tetlet.2016.09.088

  日期：2016.11

  A highly regioselective and efficient metal-free hydration of aromatic haloalkynes to α-halomethyl ketones using cheap tetrafluoroboric acid as catalyst is described. The protocol is conducted under convenient conditions and affords products in good to excellent yields, with broad substrate scope, including a variety of aromatic alkynyl chlorides, alkynyl bromides, and alkynyl iodides.

  描述了使用廉价的四氟硼酸作为催化剂的芳香族卤代炔烃的高度区域选择性和有效的无金属水合为α-卤代甲基酮。该方案是在方便的条件下进行的，并以良好的收率提供优良的产品，具有广泛的底物范围，包括各种芳族炔基氯，炔基溴化物和炔基碘化物。
• α-Chlorination of Aromatic Acetyl Derivatives with Benzyltrimethylammonium Dichloroiodate
  作者：Shoji Kajigaeshi、Takaaki Kakinami、Masayuki Moriwaki、Shizuo Fujisaki、Kimihiro Maeno、Tsuyoshi Okamoto

  DOI：10.1055/s-1988-27633

  日期：——

  Reaction of aromatic acetyl derivatives with benzyltrimethylammonium dichloroiodate in refluxing dichloroethane/methanol for several hours gave α-chloroacetyl derivatives in good yields.

  在回流二氯乙烷/甲醇中，芳香族乙酰衍生物与苄基三甲基二氯碘酸铵反应数小时，可获得高产率的α-氯乙酰衍生物。
• Media controlled photo-Favorskii type rearrangement of α-chloro acetophenones: Synthesis of phenylacetic acids
  作者：Dilip D. Dhavale、Vasant P. Mali、Surendra G. Sudrik、Harikisan R. Sonawane

  DOI：10.1016/s0040-4020(97)10081-3

  日期：1997.12

  Photolysis of substituted α-chloro acetophenones has been studied in different solvent systems wherein 1,2-aryl migration is found to be media controlled. Effect of substituents on the migratory aptitude and a direct access to phenylacetic acids, in practical yields, has been described.

  已经在不同的溶剂系统中研究了取代的α-氯乙酰苯的光解，其中发现1,2-芳基迁移受介质控制。已经描述了取代基对迁移能力和以实际产率直接获得苯乙酸的影响。
• Solvent-free microwave-assisted multi-component reaction for preparation of 2-amino-1-aryl-2-(cyclohex-1-enyl)ethanones as precursors of pseudoephedrine analogues
  作者：Li-Jian Ma、Tsutomu Inokuchi

  DOI：10.1039/c0cc00859a

  日期：——

  Microwave irradiation of chloroacetylarenes and enamines induced an aza-Darzens reaction followed by rearrangement of the aziridinium intermediate to give (2-amino-3-alkenoyl)arenes that were reduced selectively to syn-β-aminoalcohols as pseudo-ephedrine analogues.

  氯代乙酰苯与烯胺类的微波辐射诱导了氮杂Darzens反应，接着氮杂环丙鎓中间体的重排，得到了二氧化氨基-三碳烯酰苯类化合物，这类化合物被选择性地还原为伪麻黄碱的伪手性β-氨基醇类似物。
• The Ir-Catalyzed Asymmetric Hydrogenation of α-Halogenated Ketones Utilizing Cinchona-Alkaloid-Derived NNP Ligand to Produce (<i>R</i>)- and (<i>S</i>)-Halohydrins
  作者：Qian Chen、Hao Sun、Linlin Li、Jie Tian、Qian Xu、Nana Ma、Li Li、Lin Zhang、Chun Li

  DOI：10.1021/acs.joc.2c02109

  日期：2022.12.2

  hydrogenation of α-halogenated ketones with iridium catalyst was developed, utilizing easily accessed cinchona-alkaloid-based NNP ligands. Various α-chloroacetophenones, heterocyclic thienyl and furanyl substrates, and even bromoketones were completely converted to the desired chiral halohydrins by this protocol. Both (R)- and (S)-chiral halohydrins can be prepared by changing the configurations of the chiral

  利用易于获取的基于金鸡纳生物碱的 NNP 配体，开发了铱催化剂对 α-卤化酮的不对称氢化。通过该协议，各种 α-氯苯乙酮、杂环噻吩基和呋喃基底物，甚至溴酮完全转化为所需的手性卤代醇。( R )- 和 ( S )- 手性卤代醇都可以通过改变手性配体 NNP 的构型来制备，分别具有高达 99.6% ee（对映体过量）和 98.8% ee。此外，有效地进行了克级实验。