Cas 93574-10-8,Benzoic acid, 4-(2-methyl-4-oxo-3(4H)-quinazolinyl)-, 2-[[(phenylmethyl)amino]thioxomethyl]hydrazide

93574-10-8

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Basic information

Product Name: Benzoic acid, 4-(2-methyl-4-oxo-3(4H)-quinazolinyl)-, 2-[[(phenylmethyl)amino]thioxomethyl]hydrazide
Synonyms:
CAS NO:93574-10-8
Molecular Formula: C24H21N5O2S
Molecular Weight: 443.529
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: Benzoic acid, 4-(2-methyl-4-oxo-3(4H)-quinazolinyl)-, 2-[[(phenylmethyl)amino]thioxomethyl]hydrazide(CAS DataBase Reference)
NIST Chemistry Reference: Benzoic acid, 4-(2-methyl-4-oxo-3(4H)-quinazolinyl)-, 2-[[(phenylmethyl)amino]thioxomethyl]hydrazide(93574-10-8)
EPA Substance Registry System: Benzoic acid, 4-(2-methyl-4-oxo-3(4H)-quinazolinyl)-, 2-[[(phenylmethyl)amino]thioxomethyl]hydrazide(93574-10-8)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 93574-10-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 93574-10-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,5,7 and 4 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 93574-10:
(7*9)+(6*3)+(5*5)+(4*7)+(3*4)+(2*1)+(1*0)=148
148 % 10 = 8
So 93574-10-8 is a valid CAS Registry Number.

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93574-10-8Relevant academic research and scientific papers

Synthesis and antimicrobial activity of noval quinazolone derivatives

Habib,Khalil

, p. 982 - 985 (2007/10/02)

Three novel series of 4-oxoquinazoline derivatives were prepared and evaluated as potential antimicrobial agents. Evaluation of the antimicrobial activity of a variety of 4-substituted-1-thiosemicarbazides, 3,4-disubstituted thiazolines, and 3-substituted-5-thiazolidones reveals that the majority possess significant in vitro activity against Gram-positive organisms. Some derivatives also exhibited antifungal activity.

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