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1,2-dichloro-3-(methylthio)benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

17733-25-4

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17733-25-4 Usage

Physical state

Colorless to pale yellow liquid

Odor

Strong, pleasant

Uses

a. Chemical intermediate in the synthesis of pharmaceuticals
b. Chemical intermediate in the synthesis of dyes
c. Chemical intermediate in the synthesis of other organic compounds
d. Solvent in various industrial processes

Toxicity

Considered toxic

Health hazards

a. Skin irritation
b. Eye irritation
c. Respiratory system irritation

Safety precautions

Handle and store with proper safety measures to prevent health hazards

Check Digit Verification of cas no

The CAS Registry Mumber 17733-25-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,7,3 and 3 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 17733-25:
(7*1)+(6*7)+(5*7)+(4*3)+(3*3)+(2*2)+(1*5)=114
114 % 10 = 4
So 17733-25-4 is a valid CAS Registry Number.

17733-25-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2-dichloro-3-methylsulfanylbenzene

1.2 Other means of identification

Product number -
Other names 1,2-dichloro-3-methylthiobenzene

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:17733-25-4 SDS

17733-25-4Relevant academic research and scientific papers

ACRYLAMIDE DERIVATIVES AS VLA-1 INTEGRIN ANTAGONISTS AND USES THEREOF

-

Page/Page column 169, (2010/02/10)

Compounds that are VLA-1 integrin antagonists are disclosed. Also disclosed are compositions containing such compounds, and methods of using such compounds in treating diseases mediated, at least in part, by the VLA-1 integrin.

Electroreduction of Organic Compounds, 19. Formation of Benzoanellated Sulfur Heterocycles by Intramolecular Cathodic Cyclization of Dithiocarboxylic Esters

Gade, Thomas,Streek, Michael,Voss, Juergen

, p. 127 - 142 (2007/10/02)

Cathodic reduction of aryl (3) and benzyl (5) dithiopivaloates and related dithioesters with leaving groups at the benzene ring or a side chain yield the sulfur heterocycles 23, 30 - 32, and 34 depending on the nature of the starting material and the reaction conditions.In the case of the α-oxo-dithioester 22, thioindigo (44) is formed. - The corresponding thioamides 14, 16, and 18 show a strong tendency to reductive dehalogenation but the S,N-heterocycles 38 and 39 are also formed in minor amounts. - The formation of the rearranged products 29 - 32, and 34 isdiscussed in terms of C,S-splitting in the primarily formed radical anion and subsequent C,C-coupling of the fragments and follow-up reactions.Key Words: Dithiopivaloates, S-aryl, S-benzyl / Electroreduction

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