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13437-75-7

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13437-75-7 Usage

General Description

1-Phenyl-2-(thiobenzoyl)hydrazine is an organic compound that belongs to the class of hydrazines. It is composed of a phenyl group attached to the nitrogen atom of a hydrazine group, and a thiobenzoyl group attached to the other nitrogen atom. 1-Phenyl-2-(thiobenzoyl)hydrazine has the chemical formula C13H12N2OS and is commonly used in organic synthesis as a building block for the preparation of various derivatives. It has the potential to act as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Additionally, 1-Phenyl-2-(thiobenzoyl)hydrazine has been studied for its potential biological activities, such as its antifungal and antibacterial properties.

Check Digit Verification of cas no

The CAS Registry Mumber 13437-75-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,4,3 and 7 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 13437-75:
(7*1)+(6*3)+(5*4)+(4*3)+(3*7)+(2*7)+(1*5)=97
97 % 10 = 7
So 13437-75-7 is a valid CAS Registry Number.

13437-75-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name thiobenzoic acid N'-phenyl-hydrazide

1.2 Other means of identification

Product number -
Other names thiobenzoic acid-(N'-phenyl-hydrazide)

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:13437-75-7 SDS

13437-75-7Relevant articles and documents

Reactions with Hydrazonoyl Halides. Part 10. Formation of Thiohydrazide, Hydrazonoyl Sulfide and Arylazothiazole Derivatives

Abdelhamid, Abdou O.,Zohdi, Hussein F.,Rateb, Nora M.

, p. 144 - 145 (2007/10/03)

Hydrazonoyl halides react with α-thiocarbamoylcinnamonitrile derivatives, under alkaline conditions, to afford thiohydrazide (4), hydrazonoyl sulfide (7a,b) or arylazothiazole derivatives (9a,b), depending on the nature of the hydrazonoyl halide; a sequence leading to the formation of these products is discussed.

Studies on Organophosphorus Compounds. XXXIV. Syntheses of 2,3-Dihydro-1,3,4,2-Thiadiazaphospholes and Thiohydrazides

El-Barbary, A. A.,Scheibye, S.,Lawesson, S.-O.,Fritz, H.

, p. 597 - 602 (2007/10/02)

N'-Substituted hydrazides, 2, react with 2,4-bis(4-methoxyphenyl)-1,3,2,4-dithiadiphosphetane-2,4-disulfide, 1, in refluxing benzene to give 2,3-dihydro-1,3,4,2-thiadizaphospholes, 3; in one case also the thiohydrazide, 4e, was isolated.Benzohydrazide, 10

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