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(3R,5S,6R)-2,3,5,6-Tetrahydro-3-(p-fluorophenyl)-5,6-diphenyl-1,4-oxazin-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

144744-29-6

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144744-29-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 144744-29-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,7,4 and 4 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 144744-29:
(8*1)+(7*4)+(6*4)+(5*7)+(4*4)+(3*4)+(2*2)+(1*9)=136
136 % 10 = 6
So 144744-29-6 is a valid CAS Registry Number.

144744-29-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (3R,5S,6R)-2,3,5,6-Tetrahydro-3-(p-fluorophenyl)-5,6-diphenyl-1,4-oxazin-2-one

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:144744-29-6 SDS

144744-29-6Relevant academic research and scientific papers

Synthesis of Optically Active Arylglycines by Photolysis of Optically Active (β-Hydroxyamino) Carbene-Chromium(0) Complexes

Vernier, Jean-Michel,Hegedus, Louis S.,Miller, David B.

, p. 6914 - 6920 (2007/10/02)

Photolysis of chromium complexes having the optically active amino alcohol (1R,2S)-(-)- or (1S,2R)-(+)-2-amino-1,2-diphenylethanol as the amino group produced aryl-substituted oxazinones in good yield with reasonable diastereoselectivity.Facile separation of diastereoisomers followed by mild reductive cleavage produced several arylglycines, having either electron-donating or withdrawing groups on the aromatic ring, in good overall yield and with excellent enantiomeric excess.

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