1674-29-9

• 

• Basic information

  1. Product Name: (1,2,2-trichloroethyl)benzene
  2. Synonyms:
  3. CAS NO:1674-29-9
  4. Molecular Formula: C₈H₇Cl₃
  5. Molecular Weight: 209.5002
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 1674-29-9.mol
  9. Article Data: 7

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: 262.4°C at 760 mmHg
  3. Flash Point: 170.1°C
  4. Appearance: N/A
  5. Density: 1.329g/cm³
  6. Vapor Pressure: 0.0178mmHg at 25°C
  7. Refractive Index: 1.551
  8. Storage Temp.: N/A
  9. Solubility: N/A
  10. CAS DataBase Reference: (1,2,2-trichloroethyl)benzene(CAS DataBase Reference)
  11. NIST Chemistry Reference: (1,2,2-trichloroethyl)benzene(1674-29-9)
  12. EPA Substance Registry System: (1,2,2-trichloroethyl)benzene(1674-29-9)

• Safety Data

  1. Hazard Codes: N/A
  2. Statements: N/A
  3. Safety Statements: N/A
  4. WGK Germany:
  5. RTECS:
  6. HazardClass: N/A
  7. PackingGroup: N/A
  8. Hazardous Substances Data: 1674-29-9(Hazardous Substances Data)

• Suppliers
• Usage
• SDS
• Upstream product
• Downstream Products
• Article

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• Benzene,(1,2,2-trichloroethyl)-

  Cas No: 1674-29-9

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• Benzene,(1,2,2-trichloroethyl)- cas 1674-29-9

  Cas No: 1674-29-9

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1674-29-9 Usage

General Description

(1,2,2-trichloroethyl)benzene, also known as 1,2,2-trichloroethylbenzene, is a chemical compound with the molecular formula C8H7C13. It is a colorless liquid with a sweet, chloroform-like odor. (1,2,2-trichloroethyl)benzene is mainly used as a solvent in the production of organic chemicals and as a degreaser in some industrial applications. It is considered to be a hazardous chemical, with potential health effects including irritation of the respiratory system, skin, and eyes. Prolonged or repeated exposure to (1,2,2-trichloroethyl)benzene can also damage the liver and kidneys. Due to its potential for harm, it is important to handle and use (1,2,2-trichloroethyl)benzene with caution and in accordance with safety regulations.

Check Digit Verification of cas no

The CAS Registry Mumber 1674-29-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,7 and 4 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1674-29:
(6*1)+(5*6)+(4*7)+(3*4)+(2*2)+(1*9)=89
89 % 10 = 9
So 1674-29-9 is a valid CAS Registry Number.

1674-29-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name	1,2,2-trichloroethylbenzene

1.2 Other means of identification

Product number	-
Other names	1,2,2-trichloro-1-phenylethane

1.3 Recommended use of the chemical and restrictions on use

Identified uses	For industry use only.
Uses advised against	no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number	-
Service hours	Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1674-29-9 SDS

1674-29-9Upstream product

• 52147-97-4 trans 2-phenylethenesulfonyl chloride 
• 79-01-6 Trichloroethylene 
• 79692-77-6 (phenylazo)diphenylmethanol 
• 140-10-3 (E)-3-phenylacrylic acid 
• 35115-76-5 2,3-dichloro-3-phenyl-propionic acid 
• 622-25-3 1-(2-chlorovinyl)benzene 
• 100-42-5 styrene 
• 100-52-7 benzaldehyde 
• 6943-57-3 (phenylazo)diphenylmethyl acetate 
• 574-61-8 benzophenone N-phenylhydrazone 
• 2612-36-4 2,2-dichloro-1-phenylethanol 
• 4110-77-4 (E)-β-chlorostyrene 

1674-29-9Downstream Products

• 706-93-4 Phenylpentachloroethane 

1674-29-9Relevant articles and documents

Reaction of Styrene with Chlorine Dioxide

Loginova,Chukicheva, I. Yu.,Kuchin

, p. 825 - 828 (2018/06/14)

Reaction of styrene with chlorine dioxide under various conditions selectively produces 1-phenyl- 2-chloroethanone, with 1-phenyl-2-chloroethanol, 2-hydroxy-1-phenylethanone, (1,2-dichloroethyl)benzene, (2-chloro-1-phenyl)ethene, and (1,2,2-trichloroethyl

Quaternary ammonium polychlorides as efficient reagents for chlorination of unsaturated compounds

Zelikman,Tyurin,Smirnov,Zyk

, p. 1541 - 1546 (2007/10/03)

Chlorination of unsaturated compounds by benzyltributylammonium polychlorides results in higher yields of addition products compared to those obtained with molecular chlorine.

Reaction of α,β-Unsaturated Carboxylic Acids with Manganese(III) Acetate in the Presence of Chloride Ion

Yonemura, Hiroshi,Nishino, Hiroshi,Kurosawa, Kazu

, p. 3153 - 3160 (2007/10/02)

The reaction of 3-phenylpropenoic acids with manganese(III) acetate - Cl- complex yielded 1,2,2-trichloro-1-phenylethanes, 1-acetoxy-2,2-dichloro-1-phenylethanes, and 2,2-dichloro-1-phenylethanols. (E)-2,3-Diphenylpropenoic acids gave 2,2-dichloro-1,2-diphenylethanones and 2-acetoxy-1,2-diphenylethanones. 3,3-Diphenylpropenoic acids yielded 2,2-dichloro-1,1-diphenylethenes, 1-acetoxy-2,2-dichloro-1,1-diphenylethanes, 2,2-dichloro-1,1-diphenyl-1-ethanols, and 2-hydroxy-2,2-diphenylethanal.Fluorenylideneacetic acid gave 9-chloro-9-(dichloromethyl)fluorene, 9-acetoxy-9-(dichloromethyl)fluorene, and 9-fluorenone. 1-Cyclohexenecarboxylic acid yielded 1,2-dichlorocyclohexanecarboxylic acid and 1-acetoxy-2-chlorocyclohexanecarboxylic acid.The reaction can be explained in terms of a free-radical mechanism involving manganese(III) acetate - Cl- complexation, addition of Cl. radical, decarboxylation, and the oxidation of chloroethenes which are the reaction intermediates.

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