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(S)-2-oxo-2-((1-phenylethyl)amino)acetic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

164219-32-3

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164219-32-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 164219-32-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,4,2,1 and 9 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 164219-32:
(8*1)+(7*6)+(6*4)+(5*2)+(4*1)+(3*9)+(2*3)+(1*2)=123
123 % 10 = 3
So 164219-32-3 is a valid CAS Registry Number.

164219-32-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (S)-2-oxo-2-((1-phenylethyl)amino)acetic acid

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:164219-32-3 SDS

164219-32-3Relevant academic research and scientific papers

Supporting-Electrolyte-Free Anodic Oxidation of Oxamic Acids into Isocyanates: An Expedient Way to Access Ureas, Carbamates, and Thiocarbamates

Petti, Alessia,Fagnan, Corentin,van Melis, Carlo G. W.,Tanbouza, Nour,Garcia, Anthony D.,Mastrodonato, Andrea,Leech, Matthew C.,Goodall, Iain C. A.,Dobbs, Adrian P.,Ollevier, Thierry,Lam, Kevin

supporting information, p. 2614 - 2621 (2021/06/27)

We report a new electrochemical supporting-electrolyte-free method for synthesizing ureas, carbamates, and thiocarbamates via the oxidation of oxamic acids. This simple, practical, and phosgene-free route includes the generation of an isocyanate intermediate in situ via anodic decarboxylation of an oxamic acid in the presence of an organic base, followed by the one-pot addition of suitable nucleophiles to afford the corresponding ureas, carbamates, and thiocarbamates. This procedure is applicable to different amines, alcohols, and thiols. Furthermore, when single-pass continuous electrochemical flow conditions were used and this reaction was run in a carbon graphite Cgr/Cgr flow cell, urea compounds could be obtained in high yields within a residence time of 6 min, unlocking access to substrates that were inaccessible under batch conditions while being easily scalable.

Syntheses of morpholine-2,3-diones and 2-hydroxymorpholin-3-ones: Intermediates in the synthesis of aprepitant

Nelson, Todd D.,Rosen, Jonathan D.,Brands, Karel M.J.,Craig, Bridgette,Huffman, Mark A.,McNamara, James M.

, p. 8917 - 8920 (2007/10/03)

The preparation of morpholine-2,3-diones and 2-hydroxymorpholin-3-ones from N-substituted β-amino alcohols is reported. These were useful intermediates in the synthesis and development of aprepitant.

Enantiomerically pure amines by a new method: Biotransformation of oxalamic esters using the lipase from Candida antarctica

Chapman, Daniel T.,Crout, David H. G.,Mahmoudian, Mahmoud,Scopes, David I. C.,Smith, Paul W.

, p. 2415 - 2416 (2007/10/03)

Octyl oxalamic esters of 1-phenylethylamine and substituted 1-phenylethylamines are kinetically resolved with high stereoselectivity by lipase B from Candida antarctica.

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