60182-96-9 Usage
Uses
Used in Pharmaceutical Industry:
2-AMINO-3-METHYL-HEXANOIC ACID is used as a building block for the synthesis of pharmaceuticals, contributing to the development of new drugs and biologically active molecules.
Used in Chemical Industry:
2-AMINO-3-METHYL-HEXANOIC ACID is used as an intermediate in the production of synthetic organic compounds, facilitating the creation of various chemical products.
Used in Research and Development:
2-AMINO-3-METHYL-HEXANOIC ACID is utilized in the research and development of drugs and biologically active molecules, playing a role in the biosynthesis of natural products and exploring its potential therapeutic properties.
Used in Neurological and Metabolic Disorders Treatment:
2-AMINO-3-METHYL-HEXANOIC ACID is investigated for its potential therapeutic properties in the treatment of various neurological and metabolic disorders, offering new avenues for medical interventions and patient care.
Check Digit Verification of cas no
The CAS Registry Mumber 60182-96-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,1,8 and 2 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 60182-96:
(7*6)+(6*0)+(5*1)+(4*8)+(3*2)+(2*9)+(1*6)=109
109 % 10 = 9
So 60182-96-9 is a valid CAS Registry Number.
60182-96-9Relevant academic research and scientific papers
Synthesis of (-)-Invictolide, the Pheromone Component of the Red Imported Fire Ant
Senda, Shuji,Mori, Kenji
, p. 1379 - 1384 (2007/10/02)
(-)-Invictolide was synthesized in 16 steps from 2-methylpentanal.
PREPARATION OF THE BOTH ENANTIOMERS OF THREO-2-AMINO-3-METHYLHEXANOIC ACID BY ENZYMATIC. RESOLUTION AND THEIR CONVERSION TO OPTICALLY ACTIVE FORMS OF THREO-4-METHYLHEPTAN-3-OL, A PHEROMONE COMPONENT OF THE SMALLER EUROPEAN ELM BARK BEETLE
Mori, Kenji,Iwasawa, Hiroko
, p. 2209 - 2213 (2007/10/02)
The both enantiomers of threo-2-amino-3-methylhexanoic acid were prepared by resolving its racemic N-acetate with Aspergillus acylase.The amino acid enantiomers were converted to optically active forms of threo-4-methylheptan-3-ol, a pheromone component of Scolytus multistriatus.