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3335-34-0

1-Trichloromethyl-3-methylbenzene, also known as 3-methyl-1-(trichloromethyl)benzene or α,α,α-trichlorotoluene, is an organic compound with the chemical formula C8H7Cl3. It is a colorless liquid with a pungent odor and is derived from the substitution of three chlorine atoms on the methyl group of toluene. 1-Trichloromethyl-3-methylbenzene is used as an intermediate in the production of various chemicals, such as pesticides and pharmaceuticals. Due to its potential health and environmental risks, it is important to handle 1-Trichloromethyl-3-methylbenzene with caution, following proper safety guidelines and regulations.

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  • 3335-34-0 Structure

  • Basic information

    1. Product Name: 1-Trichloromethyl-3-methylbenzene
    2. Synonyms: 1-Trichloromethyl-3-methylbenzene
    3. CAS NO:3335-34-0
    4. Molecular Formula: C8H7Cl3
    5. Molecular Weight: 0
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 3335-34-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1-Trichloromethyl-3-methylbenzene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-Trichloromethyl-3-methylbenzene(3335-34-0)
    11. EPA Substance Registry System: 1-Trichloromethyl-3-methylbenzene(3335-34-0)

  • 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: 3335-34-0(Hazardous Substances Data)

3335-34-0 Usage

Chemical Class

Chlorobenzenes

Physical State

Colorless liquid at room temperature

Usage

Intermediate in the production of pharmaceuticals, agrochemicals, and dyes

Health Hazards

Can cause skin and eye irritation upon contact, harmful if inhaled or ingested

Check Digit Verification of cas no

The CAS Registry Mumber 3335-34-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,3 and 5 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3335-34:
(6*3)+(5*3)+(4*3)+(3*5)+(2*3)+(1*4)=70
70 % 10 = 0
So 3335-34-0 is a valid CAS Registry Number.

3335-34-0SDS

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 3-Methylbenzotrichloride

1.2 Other means of identification

Product number -
Other names 1-methyl-3-(trichloromethyl)-benzene

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:3335-34-0 SDS

3335-34-0Downstream Products

3335-34-0Relevant articles and documents

Process for the preparation of trichloromethyl-substituted aromatic compounds, and trichloromethyl-substituted aromatic compounds obtained in this process

-

, (2008/06/13)

Trichloromethyl-substituted aromatic compounds are obtained by the chlorination of thioethers of the formula STR1 wherein Ar represents an optionally substituted aryl radial, X1 denotes hydrogen or halogen, and R1 represents optionally substituted alkyl, aralkyl, the nitrile group, an optionally substituted aryl radical or the group STR2 wherein Ar and X have the meaning given. The compounds, of which some are new, can be used as intermediate products for plant protection agents.

Process for preparing substituted benzotrichlorides

-

, (2008/06/13)

The invention herein pertains to a novel process for making substituted benzotrifluorides.

Substituted Benzotrichloride Synthesis by Phase Transfer-Catalyzed Chlorination

Chupp, J. P.,Grabiak, R. C.,Leschinsky, K. L.,Neumann, T. L.

, p. 224 - 226 (2007/10/02)

A new method for converting benzyl and benzal chlorides to benzotrichlorides is reported.In contrast to prior art, the process involves contacting the substrates with strong alkali in a two-phase system containing phase transfer catalyst using organic soluble perchloralkanes acting upon base-generated carbanions.The method is particularly useful for preparing benzotrichlorides substituted by either alkyl or nitro groups.

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