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2740-95-6

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2740-95-6 Usage

General Description

1,3-dimethyl-1-phenylthiourea is a chemical compound with the molecular formula C9H12N2S. It is a thiourea compound with a phenyl group and two methyl groups attached to the nitrogen atoms. 1,3-dimethyl-1-phenylthiourea is commonly used as a catalyst in various organic reactions, including the synthesis of pharmaceuticals and agrochemicals. It is also used in the production of rubber and plastics. 1,3-dimethyl-1-phenylthiourea has been studied for its potential use as an antioxidant and has shown promising results in scavenging free radicals and inhibiting lipid peroxidation. However, it is important to handle this compound with caution as it is toxic if ingested and may cause irritation to the skin and eyes upon contact.

Check Digit Verification of cas no

The CAS Registry Mumber 2740-95-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,4 and 0 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2740-95:
(6*2)+(5*7)+(4*4)+(3*0)+(2*9)+(1*5)=86
86 % 10 = 6
So 2740-95-6 is a valid CAS Registry Number.

2740-95-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-dimethyl-1-phenylthiourea

1.2 Other means of identification

Product number -
Other names N,N-Dimethyl-N'-phenylsulfonylharnstoff

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:2740-95-6 SDS

2740-95-6Relevant articles and documents

Activation of Dithiocarbamate by 2-Halothiazolium Salts

Sugimoto, Hirohiko,Makino, Itsuo,Hirai, Kentaro

, p. 2263 - 2267 (2007/10/02)

Activation of dithiocarbamate salts with 2-halo-3-alkyl-4-phenylthiazolium salt and subsequent one-pot nucleophilic reaction with N, S, and O nucleophiles provided substituted thioureas, dithiocarbamates, and thiocarbamates or amides, respectively, under very mild conditions.A useful thiocarbonyl-transfer reaction is also described that consists of activation of imidazolodithiocarbamate and a subsequent one-pot nucleophilic reaction. (Thiocarbonyl)diimidazole is generated in situ.

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