Cas 1292290-36-8,(5-(1,3-diphenyl-1H-pyrazol-4-yl)-3-phenyl-4,5-dihydro-1H-pyrazol-1-yl)(pyridin-4-yl)methanone

1292290-36-8

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Basic information

Product Name: (5-(1,3-diphenyl-1H-pyrazol-4-yl)-3-phenyl-4,5-dihydro-1H-pyrazol-1-yl)(pyridin-4-yl)methanone
Synonyms:
CAS NO:1292290-36-8
Molecular Formula:
Molecular Weight: 469.546
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: (5-(1,3-diphenyl-1H-pyrazol-4-yl)-3-phenyl-4,5-dihydro-1H-pyrazol-1-yl)(pyridin-4-yl)methanone(CAS DataBase Reference)
NIST Chemistry Reference: (5-(1,3-diphenyl-1H-pyrazol-4-yl)-3-phenyl-4,5-dihydro-1H-pyrazol-1-yl)(pyridin-4-yl)methanone(1292290-36-8)
EPA Substance Registry System: (5-(1,3-diphenyl-1H-pyrazol-4-yl)-3-phenyl-4,5-dihydro-1H-pyrazol-1-yl)(pyridin-4-yl)methanone(1292290-36-8)

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: 1292290-36-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1292290-36-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,9,2,2,9 and 0 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1292290-36:
(9*1)+(8*2)+(7*9)+(6*2)+(5*2)+(4*9)+(3*0)+(2*3)+(1*6)=158
158 % 10 = 8
So 1292290-36-8 is a valid CAS Registry Number.

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1292290-36-8Relevant academic research and scientific papers

Synthesis and antimicrobial activity of some (3-phenyl-5-(1-phenyl-3-aryl- 1H-pyrazol-4-yl)-4,5-dihydro-1H-pyrazol-1-yl)(pyridin-4-yl)methanones: New derivatives of 1,3,5-trisubstituted pyrazolines

Kumar, Satyender,Meenakshi,Kumar, Sunil,Kumar, Parvin

, p. 433 - 439 (2013)

A series of (3-phenyl-5-(1-phenyl-3-aryl-1H-pyrazol-4-yl)-4,5-dihydro-1H- pyrazol-1-yl)(pyridin-4-yl)methanones was synthesized by condensing suitably substituted chalcones, i.e., 3-(3-aryl-1-phenyl-1H-pyrazol-4-yl)-1-phenylprop-2- en-1-ones, and isoniazi

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