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1-benzyl-3-(trifluoromethyl)piperazine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

167566-34-9

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167566-34-9 Usage

Chemical structure

Piperazine derivative with a benzyl group and a trifluoromethyl group attached to the piperazine ring

Pharmacological properties

a. Antidepressant potential
b. Anxiolytic potential

Application

a. As a precursor in organic synthesis
b. Potential use in the development of new drugs

Safety precautions

Handle with caution due to potential hazards if not used properly

Check Digit Verification of cas no

The CAS Registry Mumber 167566-34-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,7,5,6 and 6 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 167566-34:
(8*1)+(7*6)+(6*7)+(5*5)+(4*6)+(3*6)+(2*3)+(1*4)=169
169 % 10 = 9
So 167566-34-9 is a valid CAS Registry Number.

167566-34-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-benzyl-3-(trifluoromethyl)piperazine

1.2 Other means of identification

Product number -
Other names 1-BENZYL-3-TRIFLUOROMETHYL-PIPERAZINE

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:167566-34-9 SDS

167566-34-9Relevant academic research and scientific papers

BIS-HETEROARYL DERIVATIVES AS MODULATORS OF PROTEIN AGGREGATION

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Paragraph 0177, (2017/02/24)

The present invention relates to certain bis-heteroaryl compounds, pharmaceutical compositions containing them, and methods of using them, including methods for preventing, reversing, slowing, or inhibiting protein aggregation, and methods of treating diseases that are associated with protein aggregation, including neurodegenerative diseases such as Parkinson's disease, Alzheimer's disease, Lewy body disease, Parkinson's disease with dementia, fronto- temporal dementia, Huntington's Disease, amyotrophic lateral sclerosis, and multiple system atrophy, and cancer including melanoma.

5- (4- (HALOALKOXY) PHENYL) PYRIMIDINE-2-AMINE COMPOUNDS AND COMPOSITIONS AS KINASE INHIBITORS

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Page/Page column 59, (2009/04/25)

The invention provides compounds of formula (1) and pharmaceutical compositions thereof, which are useful as protein kinase inhibitors, as well as methods for using such compounds to treat, ameliorate or prevent a condition associated with abnormal or deregulated kinase activity. In some embodiments, the invention provides methods for using such compounds to treat, ameliorate or prevent diseases or disorders that involve abnormal activation of c-kit, PDGFRα, PDGFRβ, CSF1R, AbI, BCR-AbI, CSK, JNK1, JNK2, p38, p70S6K, TGFβ, SRC, EGFR, trkB, FGFR3. Fes, Lck, Syk, RAF, MKK4, MKK6, SAPK2β, BRK, Fms, KDR, c-rapor b-raf kinases.

NOVEL BENZOFURAN DERIVATIVES, WHICH CAN BE USED IN PROPHYLAXIS OR TREATMENT OF 5-HT6 RECEPTOR-RELATED DISORDER

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Page/Page column 120-121, (2010/02/12)

The present invention relates to compounds of formula (I): wherein P, R3, W1, and W2 are as described herein, to pharmaceutical compositions comprising the compounds, to processes for their preparation, as well as to the use of the compounds for the preparation of a medicament against 5-HT6 receptor-related disorders.

2-(Trifluoromethyl)piperazine: synthesis and characterization using NMR and X-ray photoelectron spectroscopy

Jenneskens, Leonardus W.,Mahy, Jan,Berg, Ellen M. M. de Brabander-van.,Hoef, Ineke van der,Lugtenburg, Johan

, p. 97 - 102 (2007/10/02)

The synthesis of 2-(trifluoromethyl)piperazine (1) is reported. 1H NMR spectroscopy shows that in the chair-type piperazine ring the CF3 group occupies an equatorial position.X-ray photoelectron spectroscopy of solid 1 reveals that the CF3 group induces a secondary (β) chemical shift of 1.5 eV on the C 1s core binding energy of its nearest neighbour carbon atom.The results are supported by semi-empirical PM3 and HAM/3 calculations.

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