Cas 871037-26-2,[2-(4-amino-5-thioxo-4,5-dihydro-1<i>H</i>-[1,2,4]triazol-3-ylmethoxy)-5-methyl-phenyl]-(3-chloro-phenyl)-methanone

871037-26-2

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Basic information

Product Name: [2-(4-amino-5-thioxo-4,5-dihydro-1H-[1,2,4]triazol-3-ylmethoxy)-5-methyl-phenyl]-(3-chloro-phenyl)-methanone
Synonyms: [2-(4-amino-5-thioxo-4,5-dihydro-1H-[1,2,4]triazol-3-ylmethoxy)-5-methyl-phenyl]-(3-chloro-phenyl)-methanone
CAS NO:871037-26-2
Molecular Formula:
Molecular Weight: 374.851
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: [2-(4-amino-5-thioxo-4,5-dihydro-1H-[1,2,4]triazol-3-ylmethoxy)-5-methyl-phenyl]-(3-chloro-phenyl)-methanone(CAS DataBase Reference)
NIST Chemistry Reference: [2-(4-amino-5-thioxo-4,5-dihydro-1H-[1,2,4]triazol-3-ylmethoxy)-5-methyl-phenyl]-(3-chloro-phenyl)-methanone(871037-26-2)
EPA Substance Registry System: [2-(4-amino-5-thioxo-4,5-dihydro-1H-[1,2,4]triazol-3-ylmethoxy)-5-methyl-phenyl]-(3-chloro-phenyl)-methanone(871037-26-2)

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: 871037-26-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 871037-26-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,1,0,3 and 7 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 871037-26:
(8*8)+(7*7)+(6*1)+(5*0)+(4*3)+(3*7)+(2*2)+(1*6)=162
162 % 10 = 2
So 871037-26-2 is a valid CAS Registry Number.

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871037-26-2Relevant academic research and scientific papers

Synthesis and antimicrobial study of novel heterocyclic compounds from hydroxybenzophenones

Khanum, Shaukath A.,Shashikanth, Sheena,Umesha,Kavitha

, p. 1156 - 1162 (2007/10/03)

The triazolothiadiazine analogues 6a-e were obtained via a multistep synthesis sequences beginning with the hydroxybenzophenones 1a-e. Hydroxybenzophenones on reaction with ethyl chloroacetate affords ethyl (2-aroylaryloxy)acetates 2a-e which on treatment

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