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1,1,1-trifluoro-2-phenylpent-4-en-2-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

133367-66-5

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133367-66-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 133367-66-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,3,6 and 7 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 133367-66:
(8*1)+(7*3)+(6*3)+(5*3)+(4*6)+(3*7)+(2*6)+(1*6)=125
125 % 10 = 5
So 133367-66-5 is a valid CAS Registry Number.

133367-66-5Downstream Products

133367-66-5Relevant academic research and scientific papers

Synthesis of 1-tetrasubstituted 2,2,2-trifluoroethylamine derivatives via palladium-catalyzed allylation of sp3 C–H bonds

Morisaki, Kazuhiro,Kondo, Yuta,Sawa, Masanao,Morimoto, Hiroyuki,Ohshima, Takashi

, p. 1089 - 1092 (2017)

This note describes the construction of tetrasubstituted carbon stereocenters via palladium-catalyzed allylation of sp3 C–H bonds of 2,2,2-trifluoroethylamine derivatives. The presence of 2-pyridyl group of the imines derived from 1-substituted-2,2,2-trifluoroethylamine was key to promoting the reaction efficiently, allowing an access to a variety of 1-allylated 2,2,2-trifluoroethylamine derivatives with tetrasubstituted carbon stereocenters.

Regio- and Enantioselective Synthesis of Trifluoromethyl-Substituted Homoallylic α-Tertiary NH2-Amines by Reactions Facilitated by a Threonine-Based Boron-Containing Catalyst

Fager, Diana C.,Hoveyda, Amir H.,Morrison, Ryan J.

supporting information, p. 11448 - 11455 (2020/05/25)

A method for catalytic regio- and enantioselective synthesis of trifluoromethyl-substituted and aryl-, heteroaryl-, alkenyl-, and alkynyl-substituted homoallylic α-tertiary NH2-amines is introduced. Easy-to-synthesize and robust N-silyl ketimin

OXIMES TRIFLUOROMETHYLEES ET ORGANOMAGNESIENS ALLYLIQUES: SYNTHESE D'HYDROXYLAMINES HOMOALLYLIQUES ET D'AMINES HOMOALLYLIQUES PRIMAIRES

Felix, C.,Laurent, A.,Lesniak, S.,Mison, P.

, p. 301 - 323 (2007/10/02)

Les organomagnesiens allyliques s'additionnent aux oximes substituees par un groupement trifluoromethyle, pour conduire a des hydroxylamines avec des rendements eleves.Une telle reaction est particuliere a ces oximes et a ces magnesiens.Les hydroxylamines obtenues ont ete transformees en amines primaires homoallyliques.

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