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α-Ketoisovalerate, also known as 2-methyl-3-oxopentanoic acid, is an organic compound that serves as an important intermediate in the metabolism of branched-chain amino acids, such as leucine, isoleucine, and valine. It is a key component in the process of deamination, which is the removal of an amino group from an amino acid, resulting in the formation of α-ketoisovalerate and ammonia. α-ketoisovalerate plays a crucial role in the citric acid cycle, also known as the Krebs cycle or tricarboxylic acid cycle, where it is converted into succinyl-CoA, which is then further metabolized to produce energy in the form of ATP. The conversion of α-ketoisovalerate to succinyl-CoA is catalyzed by the enzyme α-ketoisovalerate dehydrogenase, which is part of a multi-enzyme complex. This process is essential for energy production and maintaining cellular homeostasis.

2507-77-9

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2507-77-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2507-77-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,0 and 7 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2507-77:
(6*2)+(5*5)+(4*0)+(3*7)+(2*7)+(1*7)=79
79 % 10 = 9
So 2507-77-9 is a valid CAS Registry Number.

2507-77-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methyl-2-oxobutanoate

1.2 Other means of identification

Product number -
Other names 3-oxoisovalerate

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:2507-77-9 SDS

2507-77-9Relevant academic research and scientific papers

Thermodynamics of reactions catalysed by branched-chain-amino-acid transaminase

Tewari, Yadu B.,Goldberg, Robert N.,Rozzell, J. David

, p. 1381 - 1398 (2007/10/03)

Apparent equilibrium constants and calorimetric enthalpies of reaction have been measured for reactions catalysed by branched-chain-amino-acid transaminase. The following biochemical reactions have been studied at the temperature 298.15 K and in the pH ra

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