Cas 1160952-91-9,3,5-bis-[β-(5-{4-chloro-phenylazo}-4-hydroxy-3-methoxy-phenyl)-ethynyl]-1H-pyrazole

1160952-91-9

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Basic information

Product Name: 3,5-bis-[β-(5-{4-chloro-phenylazo}-4-hydroxy-3-methoxy-phenyl)-ethynyl]-1H-pyrazole
Synonyms: 3,5-bis-[β-(5-{4-chloro-phenylazo}-4-hydroxy-3-methoxy-phenyl)-ethynyl]-1H-pyrazole
CAS NO:1160952-91-9
Molecular Formula:
Molecular Weight: 641.513
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: 3,5-bis-[β-(5-{4-chloro-phenylazo}-4-hydroxy-3-methoxy-phenyl)-ethynyl]-1H-pyrazole(CAS DataBase Reference)
NIST Chemistry Reference: 3,5-bis-[β-(5-{4-chloro-phenylazo}-4-hydroxy-3-methoxy-phenyl)-ethynyl]-1H-pyrazole(1160952-91-9)
EPA Substance Registry System: 3,5-bis-[β-(5-{4-chloro-phenylazo}-4-hydroxy-3-methoxy-phenyl)-ethynyl]-1H-pyrazole(1160952-91-9)

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: 1160952-91-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1160952-91-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,6,0,9,5 and 2 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1160952-91:
(9*1)+(8*1)+(7*6)+(6*0)+(5*9)+(4*5)+(3*2)+(2*9)+(1*1)=149
149 % 10 = 9
So 1160952-91-9 is a valid CAS Registry Number.

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1160952-91-9Relevant academic research and scientific papers

Synthesis and evaluation of curcumin analogues as cytotoxic agents

Fadda, Ahmed A.,Badria, Farid A.,El-Attar, Khaled M.

, p. 413 - 430 (2010)

Seventeen curcumin analogues were prepared and evaluated for in vitro and in vivo cytotoxicity against an Ehrlich ascites carcinoma (EAC). In vitro results revealed that compounds 10, 7, and 12 were the most potent analogues against EAC respectively. Howe

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