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Propanamide, 3,3,3-trifluoro-2-hydroxy-N-(phenylmethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

125969-76-8

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125969-76-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 125969-76-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,9,6 and 9 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 125969-76:
(8*1)+(7*2)+(6*5)+(5*9)+(4*6)+(3*9)+(2*7)+(1*6)=168
168 % 10 = 8
So 125969-76-8 is a valid CAS Registry Number.

125969-76-8SDS

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 N-benzyl-3,3,3-trifluoro-2-hydroxypropanamide

1.2 Other means of identification

Product number -
Other names Propanamide,3,3,3-trifluoro-2-hydroxy-N-(phenylmethyl)

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:125969-76-8 SDS

125969-76-8Downstream Products

125969-76-8Relevant academic research and scientific papers

Self-disproportionation of enantiomers of 3,3,3-trifluorolactic acid amides via sublimation

Yasumoto, Manabu,Ueki, Hisanori,Soloshonok, Vadim A.

experimental part, p. 266 - 269 (2010/04/30)

Preparation of racemic and enantiomerically enriched N-phenyl- and N-benzyl-3,3,3-trifluorolactic acid amides has been developed. These compounds were found to have substantial magnitude of the self-disproportionation of enantiomers (SDE) via sublimation. For example, when N-phenyl-3,3,3-trifluorolactic acid amide of 87% ee was sublimed (12 h) from a Petri dish at 80 °C open to the atmosphere, the enantiomeric excess of the remainder increased to 96% ee. On the other hand, when a sample of the same compound of 67% ee was subjected to SDE via sublimation under the same conditions, the enantiomeric excess has decreased to 18% ee. These preliminary results as well as excellent chemical and physico-chemical characteristics of these amide derivatives render them as readily available and very promising substrates for systematic study of SDE via sublimation.

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