89459-98-3

Basic information

• Product Name: (2S,3S)-2,3-epoxy-4-methyl-1-pentanol
• Synonyms: (2S,3S)-2,3-epoxy-4-methyl-1-pentanol
• CAS NO: 89459-98-3
• Molecular Weight: 116.16
• Mol File: 89459-98-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (2S,3S)-2,3-epoxy-4-methyl-1-pentanol(CAS DataBase Reference)
• NIST Chemistry Reference: (2S,3S)-2,3-epoxy-4-methyl-1-pentanol(89459-98-3)
• EPA Substance Registry System: (2S,3S)-2,3-epoxy-4-methyl-1-pentanol(89459-98-3)

Safety Data

• Hazardous Substances Data: 89459-98-3(Hazardous Substances Data)

Upstream product

• 82290-65-1 (Z)-4-methylpent-2-en-1-ol 
• 69143-05-1 (E)-4-methyl-pent-2-en-1-ol 

Downstream Products

• 151302-40-8 (4R,5S)-3-Benzyl-4-hydroxymethyl-5-isopropyl-oxazolidin-2-one 
• 125473-34-9 (4S,5S)-5-Isopropyl-2-oxazolidinone-4-carboxylic acid 
• 125414-63-3 4-(4S)-hydroxymethyl-5-(5R)-isopropyloxazolidin-2-one 
• 151302-43-1 (4R,5S)-3-Benzyl-5-isopropyl-2-oxo-oxazolidine-4-carboxylic acid 
• 151302-41-9 (4S,5S)-3-Benzyl-5-isopropyl-2-oxo-oxazolidine-4-carboxylic acid 
• 151302-42-0 (4S,5S)-3-Benzyl-5-isopropyl-2-oxo-oxazolidine-4-carboxylic acid methyl ester 
• 87421-19-0 (2R)-2-Amino-3-hydroxy-4-methylpentansaeure-methylester 
• 87421-23-6 (2R,3S)-2-amino-3-hydroxy-4-methylpentanoic acid 
• 128053-01-0 (2S,3S)-N-benzyl-3-hydroxyleucine 
• 10148-70-6 (2S,3S)-3-hydroxyleucine 
• 481055-09-8 7a-[1-(tert-butyl-dimethyl-silanyloxy)-2-methyl-propyl]-6-methyl-3-phenyl-1,7a-dihydro-pyrrolo[1,2-c]oxazol-5-one 
• 154774-34-2 (3S,7aR)-7a-((S)-1-Hydroxy-2-methyl-propyl)-6-methyl-3-phenyl-1,7a-dihydro-pyrrolo[1,2-c]oxazol-5-one 
• 905307-89-3 (2S,3R)-1-tert-butyldimethylsilyloxy-2-(4-nitrobenzoyloxy)-3,4-dimethyl-pentane 
• 186833-31-8 7-epi-omuralide 

Relevant articles and documents

A critical outlook and comparison of enantioselective oxidation methodologies of olefins

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Amino Acids and Peptides; 70. Optically Active α-Amino Acids, N-Boc-Aminoaldehydes and α-Amino-β-hydroxy Acids from 2,3-Epoxy Alcohols

Trichloroacetimidic esters of 2,3-epoxy alcohols are transformed into oxazolines 5 and dihydrooxazines 6, respectively, depending on the structure of the educts and the catalyst.The five-membered ring compounds 5 are transformed into erythro-α-amino-β-hydroxy acids (60-70percent from epoxy alcohols) via axazolidinones 11, 12, and 13. α-Amino acids and α-substituted α-amino acids 10 as well as the corresponding aldehydes 9 are obtained from the dihydrooxazines 6 (50-60percent from epoxy alcohols).