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37088-67-8

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37088-67-8 Usage

Uses

Used in the stereoselective synthesis of phenylalanine esters drugs.

Check Digit Verification of cas no

The CAS Registry Mumber 37088-67-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,0,8 and 8 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 37088-67:
(7*3)+(6*7)+(5*0)+(4*8)+(3*8)+(2*6)+(1*7)=138
138 % 10 = 8
So 37088-67-8 is a valid CAS Registry Number.
InChI:InChI=1/C10H13NO2/c1-13-10(12)7-9(11)8-5-3-2-4-6-8/h2-6,9H,7,11H2,1H3

37088-67-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl (3R)-3-amino-3-phenylpropanoate

1.2 Other means of identification

Product number -
Other names L-|A-Phenylalanine Methyl Ester

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:37088-67-8 SDS

37088-67-8Relevant articles and documents

Multicomponent Catalytic Enantioselective Synthesis of Isoxazolidin-5-Ones

Annibaletto, Julien,Brière, Jean-Fran?ois,Levacher, Vincent,Martzel, Thomas,Oudeyer, Sylvain

supporting information, p. 4447 - 4451 (2021/08/09)

We report herein a strategy to afford a multicomponent catalytic enantioselective synthesis of β-substituted isoxazolidin-5-ones via a KMC process promoted by a suited cupreine used as bifunctional organocatalyst. The hydroxamic acid component, with a ste

Stereoselective synthesis of activated 2-arylazetidines via imino-aldol reaction

Ghorai, Manas K.,Das, Subhomoy,Das, Kalpataru,Kumar, Amit

, p. 9042 - 9049 (2015/09/01)

A simple and efficient synthetic route to substituted N-sulfinyl and N-sulfonyl azetidines is described involving imino-aldol reaction of ester enolates with racemic and non-racemic aldimines for obtaining β-amino esters as a key step. These β-amino ester

Direct catalytic asymmetric addition of acetonitrile to N-thiophosphinoylimines

Kawato, Yuji,Kumagai, Naoya,Shibasaki, Masakatsu

, p. 11227 - 11229 (2013/11/19)

Direct catalytic addition of acetonitrile pronucleophiles to thiophosphinoylimines is described. Soft Lewis acid-hard Bronsted base cooperative catalysis is crucial to promote this elusive carbon-carbon bond-forming reaction in an enantioselective fashion

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