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1H-Pyrazole, 4,5-dihydro-1,5-diphenyl-3-(trifluoromethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

966-65-4

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966-65-4 Usage

Structure

Pyrazole derivative with a trifluoromethyl group attached to the third position of the pyrazole ring

Usage

Intermediate in the synthesis of pharmaceuticals and agrochemicals

Biological activities

Anti-inflammatory and analgesic properties

Interest to researchers

Medicinal chemistry and drug discovery fields due to unique structure and potential pharmacological applications.

Check Digit Verification of cas no

The CAS Registry Mumber 966-65-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,6 and 6 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 966-65:
(5*9)+(4*6)+(3*6)+(2*6)+(1*5)=104
104 % 10 = 4
So 966-65-4 is a valid CAS Registry Number.

966-65-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-diphenyl-5-(trifluoromethyl)-3,4-dihydropyrazole

1.2 Other means of identification

Product number -
Other names 1H-Pyrazole,4,5-dihydro-1,5-diphenyl-3-(trifluoromethyl)

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:966-65-4 SDS

966-65-4Relevant academic research and scientific papers

Synthesis of Trifluoromethyl Pyrazoline and Pyrazolidine Derivatives

Nenaidenko, V. G.,Sanin, A. V.,Balenkova, E. S.

, p. 728 - 732 (2007/10/03)

Reactions of α,β-unsaturated ketones containing a trifluoromethyl group with hydrazine and alkyl-, aryl-, and dialkylhydrazines yield trifluoromethyl-substituted pyrazolidines and pyrazolines.Steric strains in the pyrazolidines facilitate their dehydratio

SYNTHESIS OF 2,2,2-TRISUBSTITUTED 5-TRIFLUOROMETHYL-Δ4-1,3,4,2-OXADIAZAPHOSPHOLINES AND THEIR POTENTIALITY AS PRECURSORS OF TRIFLUOROACETONITRILE IMINES

Tanaka, Kiyoshi,Igarashi, Toh-ru,Mitsuhashi, Keiryo

, p. 507 - 510 (2007/10/02)

N'-Phenyl- and methyltrifluoroacetohydrazides react with phosphorus pentachloride to give the corresponding 2,2,2-trichloro-3-phenyl- and methyl-Δ4-1,3,4,2-oxadiazaphospholines, from which various 2,2,2-trisubstituted derivatives are further synthesized.Heating 3-phenyl-2,2,2-tris(p-tolyloxy) analog with an excess of styrene affords 1,5-diphenyl-3-trifluoromethyl-2-pyrazoline, which indicates that the phospholine behaves as a precursor of trifluoroacetonitrile phenylimine.

PREPARATION OF TRIFLUOROACETONITRILE PHENYLAMINE AND ITS REACTIONS WITH SOME DIPOLAROPHILES

Tanaka, Kiyoshi,Maeno, Seiji,Mitsuhashi, Keiryo

, p. 543 - 546 (2007/10/02)

Trifluoroaceto-N-phenylhydrazonoyl halides, the precursors of trifluoroacetonitrile phenylamine, prepared by halogenation of trifluoroacetaldehyde phenylhydrazon, react with various olefins and acetylenes in the presence of triethylamine to give 3-trifluo

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