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1-benzoyl-3-(2-bromo-4-methyl-phenyl)-thiourea is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

446831-64-7

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446831-64-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 446831-64-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,6,8,3 and 1 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 446831-64:
(8*4)+(7*4)+(6*6)+(5*8)+(4*3)+(3*1)+(2*6)+(1*4)=167
167 % 10 = 7
So 446831-64-7 is a valid CAS Registry Number.

446831-64-7SDS

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 N-((2-bromo-4-methylphenyl)carbamothioyl)benzamide

1.2 Other means of identification

Product number -
Other names -

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:446831-64-7 SDS

446831-64-7Downstream Products

446831-64-7Relevant academic research and scientific papers

Synthesis of some new 2,4-disubstituted thiazoles as possible antibacterial and anti-inflammatory agents

Holla, B. Shivarama,Malini,Rao, B. Sooryanarayana,Sarojini,Kumari, N. Suchetha

, p. 313 - 318 (2007/10/03)

A series of arylthioureas (1), aromatic aldehyde thiosemicarbazones (2) and 5-aryl-2-furfuraldehyde thiosemicarbazones (3) were condensed with 2,4-dichloro-5-fluorophenacyl bromide to yield respective arylaminothiazoles, arylidene/5-aryl-2-furfurylidene hydrazinothiazoles (4). The newly synthesized compounds were characterized by IR, 1H-NMR and mass spectral studies. These compounds were also screened for their antibacterial and anti-inflammatory activities. Two of the newly synthesized compounds showed anti-inflammatory activity comparable with that of Ibuprofen.

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