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1-(4-DIMETHYLAMINOPHENYL)-2,2,2-TRIFLUOROETHYLAMINE is a synthetic chemical compound with the molecular formula C12H15F3N. It belongs to the class of amines, which are organic compounds derived from ammonia by replacing one or more hydrogen atoms with alkyl or aryl groups. This specific compound features a trifluoroethylamine group and a dimethylaminophenyl group, both of which contribute to its unique chemical properties. Its potential uses in chemical and pharmaceutical industries can be further explored through research and experimentation.

511522-41-1

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511522-41-1 Usage

Uses

Used in Chemical Industry:
1-(4-DIMETHYLAMINOPHENYL)-2,2,2-TRIFLUOROETHYLAMINE is used as a chemical intermediate for the synthesis of various compounds due to its unique functional groups, which can be utilized in the development of new materials and products.
Used in Pharmaceutical Industry:
1-(4-DIMETHYLAMINOPHENYL)-2,2,2-TRIFLUOROETHYLAMINE is used as a building block in the design and synthesis of new pharmaceutical agents, potentially targeting specific biological pathways or receptors for therapeutic applications.

Check Digit Verification of cas no

The CAS Registry Mumber 511522-41-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,1,1,5,2 and 2 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 511522-41:
(8*5)+(7*1)+(6*1)+(5*5)+(4*2)+(3*2)+(2*4)+(1*1)=101
101 % 10 = 1
So 511522-41-1 is a valid CAS Registry Number.

511522-41-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(1-amino-2,2,2-trifluoroethyl)-N,N-dimethylaniline

1.2 Other means of identification

Product number -
Other names S14-2724

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:511522-41-1 SDS

511522-41-1Downstream Products

511522-41-1Relevant academic research and scientific papers

BF3-promoted aromatic substitution of N-alkyl α-trifluoromethylated imine: Facile synthesis of 1-aryl-2,2,2-trifluoroethylamines

Gong, Yuefa,Kato, Katsuya,Kimoto, Hiroshi

, p. 2637 - 2645 (2007/10/03)

The aromatic substitution of three representative N-alkyl trifluoromethyl imines 1a-c (R: a, benzyl; b, benzhydryl; c, methyl), obtained from primary alkyl amines and trifluoroacetaldehyde ethyl hemiacetal, was used to investigate the preparation of 1-aryl-2,2,2-trifluoroethylamines. In the presence of BF3·OEt2, the reaction of imine 1 with various aromatic compounds proceeded smoothly at room temperature, giving N-alkyl-1-aryl-2,2,2-trifluoroethylamines in moderate-to-high yields. Moreover, successful regioselective removal of N-benzyl and N-benzhydryl groups was achieved by hydrolysis in hydrochloric acid or by palladium-catalyzed hydrogenolysis.

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