Cas 478030-39-6,1-(4-FLUOROBENZYL)-2-(TRIFLUOROMETHYL)-1H-1,3-BENZIMIDAZOLE

478030-39-6

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Basic information

Product Name: 1-(4-FLUOROBENZYL)-2-(TRIFLUOROMETHYL)-1H-1,3-BENZIMIDAZOLE
Synonyms: 1-(4-FLUOROBENZYL)-2-(TRIFLUOROMETHYL)-1H-1,3-BENZIMIDAZOLE;1-[(4-fluorophenyl)methyl]-2-(trifluoromethyl)-1H-1,3-benzodiazole
CAS NO:478030-39-6
Molecular Formula: C₁₅H₁₀F₄N₂
Molecular Weight: 294.25
EINECS: N/A
Product Categories: N/A
Mol File: 478030-39-6.mol

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 1-(4-FLUOROBENZYL)-2-(TRIFLUOROMETHYL)-1H-1,3-BENZIMIDAZOLE(CAS DataBase Reference)
NIST Chemistry Reference: 1-(4-FLUOROBENZYL)-2-(TRIFLUOROMETHYL)-1H-1,3-BENZIMIDAZOLE(478030-39-6)
EPA Substance Registry System: 1-(4-FLUOROBENZYL)-2-(TRIFLUOROMETHYL)-1H-1,3-BENZIMIDAZOLE(478030-39-6)

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: 478030-39-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 478030-39-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,8,0,3 and 0 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 478030-39:
(8*4)+(7*7)+(6*8)+(5*0)+(4*3)+(3*0)+(2*3)+(1*9)=156
156 % 10 = 6
So 478030-39-6 is a valid CAS Registry Number.

478030-39-6Upstream product

478030-39-6Downstream Products

478030-39-6Relevant academic research and scientific papers

Copper-catalyzed tandem C-N bond formation reaction: Selective synthesis of 2-(trifluoromethyl)benzimidazoles

Chen, Mu-Wang,Zhang, Xing-Guo,Zhong, Ping,Hu, Mao-Lin

experimental part, p. 1431 - 1436 (2009/12/08)

A highly practical method for the synthesis of fluorinated benzimidazoles was developed by CuI/TMEDA-catalyzed cross-coupling reaction of N-(2-haloaryl)trifluoroacetimidoyl chlorides with primary amines. The present double amination process tolerates the

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