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(4S)-2-Ethyl-5α-phenyl-2-oxazoline-4β-methanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

51594-33-3

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51594-33-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51594-33-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,5,9 and 4 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 51594-33:
(7*5)+(6*1)+(5*5)+(4*9)+(3*4)+(2*3)+(1*3)=123
123 % 10 = 3
So 51594-33-3 is a valid CAS Registry Number.

51594-33-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (4S,5S)-(-)-2-ethyl-4-hydroxymethyl-5-phenyl-2-oxazoline

1.2 Other means of identification

Product number -
Other names (4S,5S)-2-Ethyl-4-hydroxymethyl-5-phenyl-1,3-oxazolin

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:51594-33-3 SDS

51594-33-3Relevant academic research and scientific papers

Stereo-selective synthesis of 2-aryl-propionic acids of high optical purity by using chiral oxazolines

-

, (2008/06/13)

The present invention relates to a stereospecific chemical synthesis of optically pure enantiomers of 2-aryl-alkanoic acids, especially those of the biologically active (S)-aryl-propionic acids, in good chemical yields, useful for preparing large quantities thereof, and having a high optical purity.

2-OXAZOLINES FROM AMIDES VIA IMIDATES

Meyers, A. I.,Hanagan, Mary Ann,Mazzu, Arthur L.

, p. 361 - 367 (2007/10/02)

Chiral oxazolines useful in asymmetric synthesis of o-substituted phthalides and benzoic acids are readily prepared from the benzamides via their imino ethers.

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