13437-75-7 Usage
Class
Organic compound
Explanation
1-Phenyl-2-(thiobenzoyl)hydrazine is an organic compound as it is primarily composed of carbon, hydrogen, and nitrogen atoms.
Explanation
The chemical formula represents the composition of the compound, with 13 carbon atoms, 12 hydrogen atoms, 2 nitrogen atoms, 1 oxygen atom, and 1 sulfur atom.
Explanation
The compound consists of a phenyl group (a ring with a side chain) attached to one nitrogen atom of a hydrazine group (NH-NH2), and a thiobenzoyl group (a thioester with a benzene ring) attached to the other nitrogen atom.
Explanation
1-Phenyl-2-(thiobenzoyl)hydrazine is commonly used as a building block in organic synthesis for the preparation of various derivatives.
Explanation
The compound has the potential to act as an intermediate in the synthesis of pharmaceuticals and agrochemicals, which can be used in the development of drugs and pesticides.
Explanation
1-Phenyl-2-(thiobenzoyl)hydrazine has been studied for its potential biological activities, including its ability to inhibit the growth of fungi and bacteria.
Structure
Phenyl group and thiobenzoyl group attached to hydrazine
Usage
Building block in organic synthesis
Potential applications
Intermediate in pharmaceuticals and agrochemicals
Biological activities
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.
13437-75-7Relevant 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