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Butanoic acid, 3-(phenylamino)-, methyl ester, (R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

63430-94-4

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63430-94-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 63430-94-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,4,3 and 0 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 63430-94:
(7*6)+(6*3)+(5*4)+(4*3)+(3*0)+(2*9)+(1*4)=114
114 % 10 = 4
So 63430-94-4 is a valid CAS Registry Number.

63430-94-4SDS

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 methyl (3R)-3-anilinobutanoate

1.2 Other means of identification

Product number -
Other names Butanoic acid,3-(phenylamino)-,methyl ester,(R)

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:63430-94-4 SDS

63430-94-4Downstream Products

63430-94-4Relevant academic research and scientific papers

Synthesis of N-phenyl β-amino acids via iridium-catalyzed asymmetric hydrogenation using mixed monodentate ligands

Mrsic, Natasa,Panella, Lavinia,Minnaard, Adriaan J.,Feringa, Ben L.,De Vries, Johannes G.

scheme or table, p. 36 - 39 (2011/04/18)

The iridium-catalyzed asymmetric hydrogenation of N-phenyl-β- dehydroamino acid derivatives was examined using monodentate phosphoramidite ligands. The highest yields and enantioselectivities were obtained using a mixed ligand approach with PipPhos L1 and

Production method for optically active N-aryl-beta-amino acid compounds

-

Page 8, (2010/02/08)

In a method suitable for industrial application, an optically active N-aryl-β-amino acid compound is produced by the reaction of an aromatic amine and an optically active sulfonylated β-hydroxycarboxylic acid compound. The latter can be easily derived from a β-keto carboxylic acid compound.

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