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(2R,3S)-2-Amino-3-hydroxy-pentanoic acid ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62772-39-8

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62772-39-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62772-39-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,7,7 and 2 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 62772-39:
(7*6)+(6*2)+(5*7)+(4*7)+(3*2)+(2*3)+(1*9)=138
138 % 10 = 8
So 62772-39-8 is a valid CAS Registry Number.

62772-39-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name erythro-(2S,3RS)-ethyl 2-amino-3-hydroxy-pentanoate

1.2 Other means of identification

Product number -
Other names (+/-)-threo-2-Amino-3-hydroxy-valeriansaeure-aethylester

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:62772-39-8 SDS

62772-39-8Relevant academic research and scientific papers

A simple route to syn α-amino-β-hydroxy-esters by C-2 regioselective opening of α,β-epoxy esters with metal halides

Righi,Rumboldt,Bonini

, p. 13401 - 13408 (1995)

α,β-Epoxy esters are opened by NaX (X=I, Br) in a regio and stereoselective fashion to β-hydroxy-α-halo esters, which represent suitable precursors of syn α-amino-β-hydroxy esters and β-hydroxy esters.

Synthesis, structure-activity, and structure-stability relationships of 2-substituted-n-(4-oxo-3-oxetanyl) n-acylethanolamine acid amidase (NAAA) inhibitors

Vitale, Romina,Ottonello, Giuliana,Petracca, Rita,Bertozzi, Sine Mandrup,Ponzano, Stefano,Armirotti, Andrea,Berteotti, Anna,Dionisi, Mauro,Cavalli, Andrea,Piomelli, Daniele,Bandiera, Tiziano,Bertozzi, Fabio

supporting information, p. 323 - 336 (2014/04/03)

N-Acylethanolamine acid amidase (NAAA) is a cysteine amidase that preferentially hydrolyzes saturated or monounsaturated fatty acid ethanolamides (FAEs), such as palmitoylethanolamide (PEA) and oleoylethanolamide (OEA), which are endogenous agonists of nu

DISUBSTITUTED BETA-LACTONES AS INHIBITORS OF N-ACYLETHANOLAMINE ACID AMIDASE (NAAA)

-

Paragraph 0376, (2013/06/06)

The present invention provides compounds and pharmaceutical compositions for inhibiting N-acylethanolamine acid amidase (NAAA). Inhibition of NAAA is contemplated as a method to sustain the levels of palmitoylethanolamide (PEA) and oleylethanolamide (OEA), two substrates of NAAA, in conditions characterized by reduced concentrations of PEA and OEA. The invention also provides methods for treating inflammatory diseases and pain, and other disorders in which decreased levels of PEA and OEA are associated with the disorder.

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