5619-06-7

Basic information

• Product Name: DL-ISOLEUCINE METHYL ESTER HYDROCHLORIDE
• Synonyms: METHYL 2-AMINO-3-METHYLPENTANOATE HYDROCHLORIDE;H-DL-ILE-OME HCL;DL-ISOLEUCINE METHYL ESTER HYDROCHLORIDE
• CAS NO: 5619-06-7
• Molecular Formula: C₇H₁₅NO₂*ClH
• Molecular Weight: 181.66
• Mol File: 5619-06-7.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: DL-ISOLEUCINE METHYL ESTER HYDROCHLORIDE(CAS DataBase Reference)
• NIST Chemistry Reference: DL-ISOLEUCINE METHYL ESTER HYDROCHLORIDE(5619-06-7)
• EPA Substance Registry System: DL-ISOLEUCINE METHYL ESTER HYDROCHLORIDE(5619-06-7)

Safety Data

• Hazardous Substances Data: 5619-06-7(Hazardous Substances Data)

Upstream product

• 67-56-1 methanol 
• 319-78-8 isoleucine 
• 3054-37-3 DL-isoleucine hydrochloride 
• 73-32-5 DL-isoleucine 

Downstream Products

• 1357176-48-7 N-(2,4,6-trichlorobenzoyl)-D-allo-isoleucine allyl ester 
• 1426066-77-4 methyl N-methyl-N-benzyl-2-amino-3-methylpentanoate 

Relevant articles and documents

Ligand-Enabled γ-C(sp3)–H Acetoxylation of Triflyl-Protected Amines

A palladium-catalyzed γ-C(sp3)–H acetoxylation of triflyl-protected amines has been achieved. The use of pyridine or 2-alkoxyquinoline-type ligands is key to the success of this transformation. The reaction is highly diastereoselective and easily scalable, and constitutes a direct approach for the synthesis of γ-hydroxy-α-amino acids and β,γ-dihydroxy amines, which are not readily accessible by other routes.

Highly tunable arylated cinchona alkaloids as bifunctional catalysts

We report the design and evaluation of a library of chiral bifunctional organocatalysts in which the distance between the catalytically active units can be systematically varied.