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N-Acetyl-DL-valine ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

56430-36-5

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56430-36-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56430-36-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,4,3 and 0 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 56430-36:
(7*5)+(6*6)+(5*4)+(4*3)+(3*0)+(2*3)+(1*6)=115
115 % 10 = 5
So 56430-36-5 is a valid CAS Registry Number.

56430-36-5SDS

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 (RS)-N-acetyl valine ethyl ester

1.2 Other means of identification

Product number -
Other names N-Acetyl-DL-valin-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:56430-36-5 SDS

56430-36-5Relevant academic research and scientific papers

Non-covalent immobilization of homogeneous cationic chiral rhodium-phosphine catalysts on silica surfaces

De Rege,Morita,Ott,Tumas,Broene

, p. 1797 - 1798 (2000)

Non-covalent immobilization of [(R,R)-Me-(DuPHOS)Rh-(COD)]OTf by interaction of the triflate counter ion with surface silanols of silica supports leads to an active, stable, enantioselective, asymmetric hydrogenation catalyst.

Concurrent esterification and N-acetylation of amino acids with orthoesters: A useful reaction with interesting mechanistic implications

Gibson, Sarah,Romero, Dickie,Jacobs, Hollie K.,Gopalan, Aravamudan S.

scheme or table, p. 6737 - 6740 (2011/02/25)

The concurrent esterification and N-acetylation of amino acids has been studied with triethyl orthoacetate (TEOA) and triethyl orthoformate (TEOF). In a surprising finding, only 1 equiv of TEOA in refluxing toluene was necessary to convert l-proline and l-phenylalanine into the corresponding N-acetyl ethyl esters in good yield. The same transformation using TEOF was not effective. Stereochemical outcome and stoichiometric studies as well as structural variation of the amino acids in this reaction provided unexpected mechanistic insight.

ANTI-ODOR COMPOSITIONS AND THERAPEUTIC USE

-

, (2008/06/13)

This application discloses a composition comprising a malodor compound and an anti-odor ingredient effective for reducing the presence or production of malodor. The composition may be topically applied to a subject and is useful for cosmetic conditions, pharmaceutical indications, or other objectives.

ENANTIOSELECTIVE HYDROLYSIS BY BAKER'S YEAST - II. ESTERS OF N-ACETYL AMINO ACIDS

Glaenzer, B. I.,Faber, K.,Griengl, H.

, p. 771 - 778 (2007/10/02)

D-N-Acetyl amino acid esters were obtained via enantioselective hydrolysis of their racemates by use of fermenting yeast.Evidence is given that proteinases are the enzymes involved.

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