Cas 1312677-91-0,N-(2-hydroxyphenyl) 1-(4-nitrophenyl)-4,5-dihydro-1H-1,2,3-triazole-4-carboxamide

1312677-91-0

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Basic information

Product Name: N-(2-hydroxyphenyl) 1-(4-nitrophenyl)-4,5-dihydro-1H-1,2,3-triazole-4-carboxamide
Synonyms: N-(2-hydroxyphenyl) 1-(4-nitrophenyl)-4,5-dihydro-1H-1,2,3-triazole-4-carboxamide
CAS NO:1312677-91-0
Molecular Formula:
Molecular Weight: 327.299
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: N-(2-hydroxyphenyl) 1-(4-nitrophenyl)-4,5-dihydro-1H-1,2,3-triazole-4-carboxamide(CAS DataBase Reference)
NIST Chemistry Reference: N-(2-hydroxyphenyl) 1-(4-nitrophenyl)-4,5-dihydro-1H-1,2,3-triazole-4-carboxamide(1312677-91-0)
EPA Substance Registry System: N-(2-hydroxyphenyl) 1-(4-nitrophenyl)-4,5-dihydro-1H-1,2,3-triazole-4-carboxamide(1312677-91-0)

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: 1312677-91-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1312677-91-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,2,6,7 and 7 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1312677-91:
(9*1)+(8*3)+(7*1)+(6*2)+(5*6)+(4*7)+(3*7)+(2*9)+(1*1)=150
150 % 10 = 0
So 1312677-91-0 is a valid CAS Registry Number.

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1312677-91-0Relevant academic research and scientific papers

A combined experimental and theoretical study of the thermal cycloaddition of aryl azides with activated alkenes

Zeghada, Sarah,Bentabed-Ababsa, Ghenia,Derdour, Aicha,Abdelmounim, Safer,Domingo, Luis R.,Saez, Jose A.,Roisnel, Thierry,Nassar, Ekhlass,Mongin, Florence

experimental part, p. 4295 - 4305 (2011/07/08)

Reactions were performed from aryl azides on the one hand, and activated alkenes coming from β-dicarbonyl compounds or malonodinitrile on the other hand, either with recourse to conventional heating or to microwave activation, to afford 1-aryl-1H-1,2,3-tr

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