Cas 1275578-51-2,2-(1H-benzo[d]imidazol-2-ylthio)-1-(4-((4-chlorophenyl)(phenyl)methyl)piperazin-1-yl)ethanone

1275578-51-2

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Basic information

Product Name: 2-(1H-benzo[d]imidazol-2-ylthio)-1-(4-((4-chlorophenyl)(phenyl)methyl)piperazin-1-yl)ethanone
Synonyms: 2-(1H-benzo[d]imidazol-2-ylthio)-1-(4-((4-chlorophenyl)(phenyl)methyl)piperazin-1-yl)ethanone
CAS NO:1275578-51-2
Molecular Formula:
Molecular Weight: 477.03
EINECS: N/A
Product Categories: N/A
Mol File: 1275578-51-2.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-(1H-benzo[d]imidazol-2-ylthio)-1-(4-((4-chlorophenyl)(phenyl)methyl)piperazin-1-yl)ethanone(CAS DataBase Reference)
NIST Chemistry Reference: 2-(1H-benzo[d]imidazol-2-ylthio)-1-(4-((4-chlorophenyl)(phenyl)methyl)piperazin-1-yl)ethanone(1275578-51-2)
EPA Substance Registry System: 2-(1H-benzo[d]imidazol-2-ylthio)-1-(4-((4-chlorophenyl)(phenyl)methyl)piperazin-1-yl)ethanone(1275578-51-2)

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: 1275578-51-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1275578-51-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,7,5,5,7 and 8 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1275578-51:
(9*1)+(8*2)+(7*7)+(6*5)+(5*5)+(4*7)+(3*8)+(2*5)+(1*1)=192
192 % 10 = 2
So 1275578-51-2 is a valid CAS Registry Number.

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1275578-51-2Relevant articles and documents

Synthesis of azole-containing piperazine derivatives and evaluation of their antibacterial, antifungal and cytotoxic activities

Gan, Lin-Ling,Fang, Bo,Zhou, Cheng-He

, p. 3684 - 3692 (2011/10/02)

A series of azole-containing piperazine derivatives have been designed and synthesized. The obtained compounds were investigated in vitro for their antibacterial, antifungal and cytotoxic activities. The preliminary results showed that most compounds exhi

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