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D-2-AMINO-2-PHENYLACETAMIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

63291-39-4

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63291-39-4 Usage

Chemical Properties

White powder

Check Digit Verification of cas no

The CAS Registry Mumber 63291-39-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,2,9 and 1 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 63291-39:
(7*6)+(6*3)+(5*2)+(4*9)+(3*1)+(2*3)+(1*9)=124
124 % 10 = 4
So 63291-39-4 is a valid CAS Registry Number.
InChI:InChI=1/C8H10N2O.ClH/c9-7(8(10)11)6-4-2-1-3-5-6;/h1-5,7H,9H2,(H2,10,11);1H/t7-;/m1./s1

63291-39-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R)-2-amino-2-phenylacetamide,hydrochloride

1.2 Other means of identification

Product number -
Other names D-2-Amino-2-phenylacetamide hydrochloride

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:63291-39-4 SDS

63291-39-4Relevant academic research and scientific papers

Diastereoselective formation of α-aminoamides from carbamoylsilanes and aldehyde imines

Chen, Jianxin,Pandey, Rajesh K.,Cunico, Robert F.

, p. 941 - 947 (2005)

Diastereoselectivities were determined for the reaction of a series of aldehyde imines with carbamoylsilanes, each containing chiral auxiliaries at nitrogen. A maximum de of 88% was achieved via a matched double differentiation.

STEREOSELECTIVE SYNTHESIS OF METYROSINE

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Page/Page column 12, (2011/05/08)

Provided herein are compositions including diastereomers in substantially diastereomerically pure form and enantiomers in substantially enantiomerically pure form, and processes for preparing them and converting them to metyrosine.

COMPOSITIONS AND METHODS FOR CYCLOFRUCTANS AS SEPARATION AGENTS

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Page/Page column 45-49; 60, (2010/12/31)

The present invention relates to derivatized cyclofructan compounds, compositions comprising derivatized cyclofructan compounds, and methods of using compositions comprising derivatized cyclofructan compounds for chromatographic separations of chemical species, including enantiomers. Said compositions may comprise a solid support and/or polymers comprising derivatized cyclofructan compounds.

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