Cas 1352406-65-5,(4-bromophenyl)[1-(4-chlorophenyl)-5-(trifluoromethyl)-1H-1,2,3-triazol-4-yl]methanone

1352406-65-5

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Basic information

Product Name: (4-bromophenyl)[1-(4-chlorophenyl)-5-(trifluoromethyl)-1H-1,2,3-triazol-4-yl]methanone
Synonyms: (4-bromophenyl)[1-(4-chlorophenyl)-5-(trifluoromethyl)-1H-1,2,3-triazol-4-yl]methanone
CAS NO:1352406-65-5
Molecular Formula:
Molecular Weight: 430.611
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-bromophenyl)[1-(4-chlorophenyl)-5-(trifluoromethyl)-1H-1,2,3-triazol-4-yl]methanone(CAS DataBase Reference)
NIST Chemistry Reference: (4-bromophenyl)[1-(4-chlorophenyl)-5-(trifluoromethyl)-1H-1,2,3-triazol-4-yl]methanone(1352406-65-5)
EPA Substance Registry System: (4-bromophenyl)[1-(4-chlorophenyl)-5-(trifluoromethyl)-1H-1,2,3-triazol-4-yl]methanone(1352406-65-5)

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: 1352406-65-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1352406-65-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,2,4,0 and 6 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1352406-65:
(9*1)+(8*3)+(7*5)+(6*2)+(5*4)+(4*0)+(3*6)+(2*6)+(1*5)=135
135 % 10 = 5
So 1352406-65-5 is a valid CAS Registry Number.

1352406-65-5Upstream product

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1352406-65-5Relevant academic research and scientific papers

Regioselective synthesis of 5-trifluoromethyl-1,2,3-triazoles via CF 3-directed cyclization of 1-trifluoromethyl-1,3-dicarbonyl compounds with azides

Rozin, Yury A.,Leban, Johann,Dehaen, Wim,Nenajdenko, Valentine G.,Muzalevskiy, Vasiliy M.,Eltsov, Oleg S.,Bakulev, Vasiliy A.

, p. 614 - 618 (2012)

1-Trifluoromethyl-substituted 1,3-dicarbonyl compounds are shown to undergo 100% regioselective cyclization in reactions with alkyl and aryl azides to form 4-acyl-5-trifluoromethyl-1,2,3-triazoles. The reaction represents a general method for the synthesi

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