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Piperazine, 1-(phenylmethyl)-4-[2,2,2-trifluoro-1-[(trimethylsilyl)oxy]ethyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

321573-95-9

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321573-95-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 321573-95-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,1,5,7 and 3 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 321573-95:
(8*3)+(7*2)+(6*1)+(5*5)+(4*7)+(3*3)+(2*9)+(1*5)=129
129 % 10 = 9
So 321573-95-9 is a valid CAS Registry Number.

321573-95-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-benzyl-4-(2,2,2-trifluoro-1-(trimethylsilyloxy)ethyl)piperazine

1.2 Other means of identification

Product number -
Other names -

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:321573-95-9 SDS

321573-95-9Relevant academic research and scientific papers

Nuclear Hormone Receptor Modulators

-

Page/Page column 81-82, (2012/09/25)

The invention provides a compound of Formula (I) pharmaceutically acceptable salts, pro-drugs, biologically active metabolites, stereoisomers and isomers thereof wherein the variable are defined herein. The compounds of the invention are useful for treati

New stable reagents for the nucleophilic trifluoromethylation. Part 2: Trifluoromethylation with silylated hemiaminals of trifluoroacetaldehyde

Billard,Langlois,Blond

, p. 8777 - 8780 (2007/10/03)

New reagents for the nucleophilic trifluoromethylation have been easily synthesized from fluoral hemiketal. They provide silylated trifluoromethylcarbinol from non-enolizable carbonyl compounds. (C) 2000 Elsevier Science Ltd.

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