Cas 1246473-57-3,ethyl 5-phenyl-1-(4-(trifluoromethyl)phenyl)-1H-1,2,3-triazole-4-carboxylate

1246473-57-3

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Basic information

Product Name: ethyl 5-phenyl-1-(4-(trifluoromethyl)phenyl)-1H-1,2,3-triazole-4-carboxylate
Synonyms: ethyl 5-phenyl-1-(4-(trifluoromethyl)phenyl)-1H-1,2,3-triazole-4-carboxylate
CAS NO:1246473-57-3
Molecular Formula:
Molecular Weight: 361.323
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: ethyl 5-phenyl-1-(4-(trifluoromethyl)phenyl)-1H-1,2,3-triazole-4-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: ethyl 5-phenyl-1-(4-(trifluoromethyl)phenyl)-1H-1,2,3-triazole-4-carboxylate(1246473-57-3)
EPA Substance Registry System: ethyl 5-phenyl-1-(4-(trifluoromethyl)phenyl)-1H-1,2,3-triazole-4-carboxylate(1246473-57-3)

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: 1246473-57-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1246473-57-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,6,4,7 and 3 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1246473-57:
(9*1)+(8*2)+(7*4)+(6*6)+(5*4)+(4*7)+(3*3)+(2*5)+(1*7)=163
163 % 10 = 3
So 1246473-57-3 is a valid CAS Registry Number.

1246473-57-3Upstream product

1246473-57-3Downstream Products

1246473-57-3Relevant academic research and scientific papers

Highly efficient and safe procedure for the synthesis of aryl 1,2,3-triazoles from aromatic amine in a continuous flow reactor

Stazi, Federica,Cancogni, Damiano,Turco, Lucilla,Westerduin, Pieter,Bacchi, Sergio

supporting information; experimental part, p. 5385 - 5387 (2010/11/02)

The Letter reports a safe and reliable synthesis of aryl 1,2,3-triazoles from the corresponding anilines via intermediate aryl azides, using a continuous process. The method was applied to a variety of substrates with good to excellent yields, without the

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