Cas 705970-78-1,2-(1-(naphthalen-1-yl)-1H-imidazol-2-ylthio)-N-o-tolylacetamide

705970-78-1

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Basic information

Product Name: 2-(1-(naphthalen-1-yl)-1H-imidazol-2-ylthio)-N-o-tolylacetamide
Synonyms: 2-(1-(naphthalen-1-yl)-1H-imidazol-2-ylthio)-N-o-tolylacetamide
CAS NO:705970-78-1
Molecular Formula:
Molecular Weight: 373.478
EINECS: N/A
Product Categories: N/A
Mol File: 705970-78-1.mol
Article Data: 1

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-(1-(naphthalen-1-yl)-1H-imidazol-2-ylthio)-N-o-tolylacetamide(CAS DataBase Reference)
NIST Chemistry Reference: 2-(1-(naphthalen-1-yl)-1H-imidazol-2-ylthio)-N-o-tolylacetamide(705970-78-1)
EPA Substance Registry System: 2-(1-(naphthalen-1-yl)-1H-imidazol-2-ylthio)-N-o-tolylacetamide(705970-78-1)

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: 705970-78-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 705970-78-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,0,5,9,7 and 0 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 705970-78:
(8*7)+(7*0)+(6*5)+(5*9)+(4*7)+(3*0)+(2*7)+(1*8)=181
181 % 10 = 1
So 705970-78-1 is a valid CAS Registry Number.

705970-78-1Upstream product

37394-93-7 2-chloro-N-(2-methylphenyl)acetamide

705970-78-1Downstream Products

705970-78-1Relevant articles and documents

Synthesis and biological evaluation of imidazole thioacetanilides as novel non-nucleoside HIV-1 reverse transcriptase inhibitors

Zhan, Peng,Liu, Xinyong,Zhu, Junjie,Fang, Zengjun,Li, Zhenyu,Pannecouque, Christophe,Clercq, Erik De

experimental part, p. 5775 - 5781 (2009/12/28)

A series of 2-(1-aryl-1H-imidazol-2-ylthio)acetamide [imidazole thioacetanilide (ITA)] derivatives were synthesized and evaluated as potent inhibitors of human immunodeficiency virus type-1 (HIV-1). Among them, the most potent HIV-1 inhibitors were 4a5 (E

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