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4439-83-2

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4439-83-2 Usage

General Description

Norvaline, 4-oxo- (9CI) is a chemical compound with the molecular formula C5H11NO2. It is a derivative of the amino acid valine and contains a ketone group, which gives it its "4-oxo" designation. Norvaline has been studied for its potential applications in various fields, including pharmaceuticals, food additives, and biochemistry. It has been shown to have antioxidative and neuroprotective effects, and may also play a role in regulating the function of enzymes involved in protein synthesis. Additionally, norvaline has been investigated for its potential to enhance muscle growth and performance in bodybuilding and athletic supplements. Overall, norvaline, 4-oxo- (9CI) is a versatile chemical with a range of potential uses and benefits.

Check Digit Verification of cas no

The CAS Registry Mumber 4439-83-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,3 and 9 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4439-83:
(6*4)+(5*4)+(4*3)+(3*9)+(2*8)+(1*3)=102
102 % 10 = 2
So 4439-83-2 is a valid CAS Registry Number.
InChI:InChI=1/C5H9NO3/c1-3(7)2-4(6)5(8)9/h4H,2,6H2,1H3,(H,8,9)/p-1

4439-83-2SDS

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 (2S)-2-amino-4-oxopentanoic acid

1.2 Other means of identification

Product number -
Other names Norvaline,4-oxo

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:4439-83-2 SDS

4439-83-2Relevant articles and documents

Jeng et al.

, p. 2898 (1974)

Synthesis of the suicide substrate D-propargylglycine stereospecifically labelled with deuterium and investigation of its oxidation by D-amino acid oxidase

Church, Nicola J.,Young, Douglas W.

, p. 1475 - 1482 (2007/10/03)

Stereospecifically deuteriated samples of D-propargylglycine 1 have been prepared by reaction of the labelled Pmc-protected aziridine free acids 22 with a lithium acetylide followed by deprotection. These samples have been used to show that D-amino acid oxidase, in converting D-propargylglycine to the lactone 5, deprotonates C-3 in a non-stereospecific manner. This strongly supports the idea that non-enzymic deprotonation is a key step in the formation of this compound.

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