Cas 292181-58-9,(1H-Benzoimidazol-2-ylsulfanyl)-acetic acid [1-(2-chloro-phenyl)-meth-(E)-ylidene]-hydrazide

292181-58-9

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Basic information

Product Name: (1H-Benzoimidazol-2-ylsulfanyl)-acetic acid [1-(2-chloro-phenyl)-meth-(E)-ylidene]-hydrazide
Synonyms: (1H-Benzoimidazol-2-ylsulfanyl)-acetic acid [1-(2-chloro-phenyl)-meth-(E)-ylidene]-hydrazide
CAS NO:292181-58-9
Molecular Formula:
Molecular Weight: 344.824
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: (1H-Benzoimidazol-2-ylsulfanyl)-acetic acid [1-(2-chloro-phenyl)-meth-(E)-ylidene]-hydrazide(CAS DataBase Reference)
NIST Chemistry Reference: (1H-Benzoimidazol-2-ylsulfanyl)-acetic acid [1-(2-chloro-phenyl)-meth-(E)-ylidene]-hydrazide(292181-58-9)
EPA Substance Registry System: (1H-Benzoimidazol-2-ylsulfanyl)-acetic acid [1-(2-chloro-phenyl)-meth-(E)-ylidene]-hydrazide(292181-58-9)

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: 292181-58-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 292181-58-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,2,1,8 and 1 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 292181-58:
(8*2)+(7*9)+(6*2)+(5*1)+(4*8)+(3*1)+(2*5)+(1*8)=149
149 % 10 = 9
So 292181-58-9 is a valid CAS Registry Number.

292181-58-9Upstream product

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292181-58-9Relevant academic research and scientific papers

Green route for the heterocyclization of 2-mercaptobenzimidazole into β-lactum segment derivatives containing -CONH- bridge with benzimidazole: Screening in vitro antimicrobial activity with various microorganisms

Desai, Krunal G.,Desai, Kishor R.

, p. 8271 - 8279 (2007/10/03)

The efficient and rapid synthesis of novel azetidin-2-ones 4a-j has been established. Thus, both microwave and conventional condensation 2-{(1H-benzimidazol)-ylthio}-N′-2-(substituted phenyl) hydrazide with chloroacetylchloride were carried out in DMF-ben

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