Cas 1451729-34-2,(4-(4-chlorophenyl)-1-(4-fluorophenyl)-3-methyl-6-(trifluoromethyl)-1H-pyrazolo[3,4-b]pyridin-5-yl)(phenyl)methanone

1451729-34-2

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Basic information

Product Name: (4-(4-chlorophenyl)-1-(4-fluorophenyl)-3-methyl-6-(trifluoromethyl)-1H-pyrazolo[3,4-b]pyridin-5-yl)(phenyl)methanone
Synonyms:
CAS NO:1451729-34-2
Molecular Formula:
Molecular Weight: 509.89
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: (4-(4-chlorophenyl)-1-(4-fluorophenyl)-3-methyl-6-(trifluoromethyl)-1H-pyrazolo[3,4-b]pyridin-5-yl)(phenyl)methanone(CAS DataBase Reference)
NIST Chemistry Reference: (4-(4-chlorophenyl)-1-(4-fluorophenyl)-3-methyl-6-(trifluoromethyl)-1H-pyrazolo[3,4-b]pyridin-5-yl)(phenyl)methanone(1451729-34-2)
EPA Substance Registry System: (4-(4-chlorophenyl)-1-(4-fluorophenyl)-3-methyl-6-(trifluoromethyl)-1H-pyrazolo[3,4-b]pyridin-5-yl)(phenyl)methanone(1451729-34-2)

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: 1451729-34-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1451729-34-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,5,1,7,2 and 9 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1451729-34:
(9*1)+(8*4)+(7*5)+(6*1)+(5*7)+(4*2)+(3*9)+(2*3)+(1*4)=162
162 % 10 = 2
So 1451729-34-2 is a valid CAS Registry Number.

1451729-34-2Upstream product

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1451729-34-2Relevant academic research and scientific papers

L-Proline-catalyzed three-component domino reactions in the regioselective synthesis of novel densely functionalized pyrazolo[3,4-b]pyridines

Gunasekaran, Pethaiah,Indumathi, Sethuraman,Perumal, Subbu

, p. 8318 - 8325 (2013)

The l-proline-catalyzed three-component synthesis of novel 3-methyl-1-aryl-1H-pyrazolo[3,4-b]pyridines in good yields from the reaction of 3-methyl-1-aryl-1H-pyrazol-5-amines, 1,3-dicarbonyl compounds and aromatic aldehydes in ethanol is described. This domino transformation presumably involves the formation of two C-C bonds and one C-N bond in a single synthetic operation.

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