Cas 199278-77-8,4-Amino-3-phenyl-2-thioxo-2,3-dihydro-thiazole-5-carboxylic acid [3-allyl-4-p-tolyl-3H-thiazol-(2Z)-ylidene]-hydrazide

199278-77-8

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Basic information

Product Name: 4-Amino-3-phenyl-2-thioxo-2,3-dihydro-thiazole-5-carboxylic acid [3-allyl-4-p-tolyl-3H-thiazol-(2Z)-ylidene]-hydrazide
Synonyms: 4-Amino-3-phenyl-2-thioxo-2,3-dihydro-thiazole-5-carboxylic acid [3-allyl-4-p-tolyl-3H-thiazol-(2Z)-ylidene]-hydrazide
CAS NO:199278-77-8
Molecular Formula:
Molecular Weight: 479.651
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: 4-Amino-3-phenyl-2-thioxo-2,3-dihydro-thiazole-5-carboxylic acid [3-allyl-4-p-tolyl-3H-thiazol-(2Z)-ylidene]-hydrazide(CAS DataBase Reference)
NIST Chemistry Reference: 4-Amino-3-phenyl-2-thioxo-2,3-dihydro-thiazole-5-carboxylic acid [3-allyl-4-p-tolyl-3H-thiazol-(2Z)-ylidene]-hydrazide(199278-77-8)
EPA Substance Registry System: 4-Amino-3-phenyl-2-thioxo-2,3-dihydro-thiazole-5-carboxylic acid [3-allyl-4-p-tolyl-3H-thiazol-(2Z)-ylidene]-hydrazide(199278-77-8)

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: 199278-77-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 199278-77-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,9,2,7 and 8 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 199278-77:
(8*1)+(7*9)+(6*9)+(5*2)+(4*7)+(3*8)+(2*7)+(1*7)=208
208 % 10 = 8
So 199278-77-8 is a valid CAS Registry Number.

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199278-77-8Relevant academic research and scientific papers

Synthesis and antimicrobial screening of some novel thiazoles, dithiazoles and thiazolylpyridines

Fahmy, Hesham Tawfik Youssef

, p. 750 - 753 (2007/10/03)

Several thiazolines 2a-c, and 4-thiazolidinones 3a-c were synthesized through the reaction of the cyanoacetic acid hydrazide derivatives la-e with phenacyl bromides or chloroacetic acid, respectively. The dithiazoles 4a, b were obtained from 2a, b through

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