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Valine, N-hydroxy-2-methyl, methyl ester (9CI) is a chemical compound with the molecular formula C7H15NO3. It is a derivative of the amino acid valine, featuring a hydroxyl group (-OH) attached to the nitrogen atom and a methyl group (-CH3) on the carbon atom at position 2. The compound is further characterized by a methyl ester group (-COOCH3) attached to the carboxylic acid group, which is a common modification in peptide chemistry to protect the carboxyl group during synthesis. This specific chemical structure is important in the context of peptide synthesis and may have applications in the development of pharmaceuticals or other bioactive compounds.

79751-33-0

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79751-33-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79751-33-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,7,5 and 1 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 79751-33:
(7*7)+(6*9)+(5*7)+(4*5)+(3*1)+(2*3)+(1*3)=170
170 % 10 = 0
So 79751-33-0 is a valid CAS Registry Number.

79751-33-0SDS

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 2-(Hydroxyamino)-2,3-dimethylbutansaeure-methylester

1.2 Other means of identification

Product number -
Other names 2-Hydroxyamino-2,3-dimethyl-butyric acid 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:79751-33-0 SDS

79751-33-0Relevant academic research and scientific papers

Synthesis and insecticidal activity of novel N-oxydihydropyrroles: 4-hydroxy-3-mesityl-1-methoxymethoxy derivatives with various substituents at the 5-position

Ito, Mitsuru,Okui, Hideshi,Nakagawa, Harumi,Mio, Shigeru,Kinoshita, Ayako,Obayashi, Takashi,Miura, Takako,Nagai, Junko,Yokoi, Shinji,Ichinose, Reiji,Tanaka, Keiji,Kodama, Seiichiro,Iwasaki, Toshiaki,Miyake, Takaaki,Takashio, Miho,Iwabuchi, Jun

, p. 761 - 768 (2007/10/03)

This paper reports the synthesis and insecticidal activity of a series of novel 4-hydroxy-3-mesityl-1-methoxymethoxy-1,5-dihydro-2H-pyrrol-2-one derivatives, in which the substituents at the 5-position were varied with a number of alkyl and spirocycloalky

Synthesis of N-Hydroxy-α-amino Acids by Alkylation of N-Benzylidene-α-amino Acid Methyl Ester N-oxides

Lau, Hans-Hermann,Schoellkopf, Ulrich

, p. 1378 - 1387 (2007/10/02)

The higher N-benzylidene-α-amino acid methyl ester N-oxides 3c-t were obtained from the lower nitrone esters 3a and b by base induced alkylation in α-position of the N->O-group.The compounds 3 were converted into the N-hydroxy-α-amino acid methyl esters 6 by heating with hydroxylamine hydrochloride in ethanol and into N-hydroxy-α-amino acids 7 with concd. hydrochloric acid. - Compound 3d was, on heating in toluene, converted to methyl 1-aza-7-oxabicycloheptanecarboxylate 8 by intramolecular cycloaddition.

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