Cas 1167437-40-2,5-[3-(trifluoromethyl)-1-(4-methoxyphenyl)-1H-pyrazol-5-yl]-3-nitropyridin-2-amine

1167437-40-2

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Basic information

Product Name: 5-[3-(trifluoromethyl)-1-(4-methoxyphenyl)-1H-pyrazol-5-yl]-3-nitropyridin-2-amine
Synonyms: 5-[3-(trifluoromethyl)-1-(4-methoxyphenyl)-1H-pyrazol-5-yl]-3-nitropyridin-2-amine
CAS NO:1167437-40-2
Molecular Formula:
Molecular Weight: 379.298
EINECS: N/A
Product Categories: N/A
Mol File: 1167437-40-2.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: 5-[3-(trifluoromethyl)-1-(4-methoxyphenyl)-1H-pyrazol-5-yl]-3-nitropyridin-2-amine(CAS DataBase Reference)
NIST Chemistry Reference: 5-[3-(trifluoromethyl)-1-(4-methoxyphenyl)-1H-pyrazol-5-yl]-3-nitropyridin-2-amine(1167437-40-2)
EPA Substance Registry System: 5-[3-(trifluoromethyl)-1-(4-methoxyphenyl)-1H-pyrazol-5-yl]-3-nitropyridin-2-amine(1167437-40-2)

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: 1167437-40-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1167437-40-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,6,7,4,3 and 7 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1167437-40:
(9*1)+(8*1)+(7*6)+(6*7)+(5*4)+(4*3)+(3*7)+(2*4)+(1*0)=162
162 % 10 = 2
So 1167437-40-2 is a valid CAS Registry Number.

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1167437-40-2Relevant articles and documents

Trifluoromethyl-substituted pyridyl- and pyrazolylboronic acids and esters: Synthesis and Suzuki-Miyaura cross-coupling reactions

Clapham, Kate M.,Batsanov, Andrei S.,Bryce, Martin R.,Tarbit, Brian

supporting information; experimental part, p. 2155 - 2161 (2009/09/04)

The synthesis of trifluoromethyl-substituted pyridylboronic acids and pyrazolylboronic esters is described via lithiation-boronation protocols (Schemes 1, 3 and 4). A study of their palladium-catalysed cross-couplings with heteroaryl halides is presented.

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