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4-methyl-N-[(3-nitrophenyl)carbamothioyl]benzamide is a complex organic chemical compound with the molecular formula C15H12N2O3S. It is characterized by the presence of a benzamide group, which is a derivative of benzoic acid, and a carbamothioyl group, which is a sulfur-containing analog of a carbamoyl group. The compound features a 4-methyl substituent on the benzamide ring and a 3-nitrophenyl group attached to the carbamothioyl moiety. This chemical is known for its potential applications in the synthesis of pharmaceuticals and agrochemicals, particularly as an intermediate in the production of certain pesticides and other chemical products. Its structure and properties make it a versatile building block in organic synthesis, although it is important to handle such compounds with care due to their potential reactivity and toxicity.

5363-15-5

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5363-15-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5363-15-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,6 and 3 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5363-15:
(6*5)+(5*3)+(4*6)+(3*3)+(2*1)+(1*5)=85
85 % 10 = 5
So 5363-15-5 is a valid CAS Registry Number.

5363-15-5SDS

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 4-Methyl-N-[(3-nitrophenyl)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

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More Details:5363-15-5 SDS

5363-15-5Upstream product

5363-15-5Downstream Products

5363-15-5Relevant academic research and scientific papers

MIGRATION TENDENCIES OF FUNCTIONAL GROUPS TOWARD SIGMATROPIC REARRANGEMENT IN 3,3-DISUBSTITUTED 3H-PYRAZOLES

Schiess, Peter,Stalder, Henri

, p. 1417 - 1420 (2007/10/02)

3,3-Disubstituted 3H-pyrazoles la - e aromatise through an intramolecular sigmatropic 1,5-(1,2-)shift of one of the quaternary groups.From a kinetic study of the uncatalysed and of the acid catalysed isomerisation reaction migration tendencies of functional groups in sigmatropic rearrangement toward neutral and toward cationic centers are obtained.

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