143216-63-1

Basic information

• Product Name: (2R,4R)-4-Amino-4-phenyl-butane-1,2-diol
• Synonyms: (2R,4R)-4-Amino-4-phenyl-butane-1,2-diol
• CAS NO: 143216-63-1
• Molecular Weight: 181.235
• Mol File: 143216-63-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (2R,4R)-4-Amino-4-phenyl-butane-1,2-diol(CAS DataBase Reference)
• NIST Chemistry Reference: (2R,4R)-4-Amino-4-phenyl-butane-1,2-diol(143216-63-1)
• EPA Substance Registry System: (2R,4R)-4-Amino-4-phenyl-butane-1,2-diol(143216-63-1)

Safety Data

• Hazardous Substances Data: 143216-63-1(Hazardous Substances Data)

Upstream product

• 620990-01-4 (4R,6S)-6-(tert-Butyl-diphenyl-silanyloxymethyl)-4-phenyl-[1,2,3]oxathiazinane 2,2-dioxide 
• 620990-00-3 sulfamic acid 1-(tert-butyl-diphenyl-silanyloxymethyl)-3-phenyl-propyl ester 
• 147976-19-0 (4S)-2,2-dimethyl-4-[(E)-2-phenylethenyl]-1,3-dioxolane 
• 157732-87-1 (4S)-2,2-dimethyl-4-(2-phenylethyl)-1,3-dioxolane 
• 124988-64-3 (S)-4-phenyl-1,2-butanediol 
• 1100-88-5 benzyltriphenylphosphonium chloride 
• 620990-03-6 Acetic acid (1R,3R)-3-benzyloxycarbonylamino-1-(tert-butyl-diphenyl-silanyloxymethyl)-3-phenyl-propyl ester 
• 143216-61-9 (2S,3S,4S)-4-amino-2,3-epoxy-4-phenyl-1-butanol 

Relevant articles and documents

Stereoselective synthesis of the 1,N2-deoxyguanosine adducts of cinnamaldehyde. A stereocontrolled route to deoxyguanosine adducts of α,β-unsaturated aldehydes

α,β-Unsaturated aldehydes (enals) react with deoxyguanosine and have mutagenic potential. For higher enals, the reaction of deoxyguanosine gives diastereomeric 6-substituted 8-hydroxypyrimidopurinone products. These stereoisomers may have different local

Chiral α,β-Epoxy Group as a Stereocontrolling Element in the Reduction of N-Metalloimines. A Short Synthesis of anti-Epoxy Amines

Reduction of the α,β-epoxy N-metalloimines generated from the TBS ether of (2S,3S)-3-cyano-2,3-epoxy-1-propanol (1), Grignard reagents, and Me3SiCl with NaBH4 afforded the TBS ethers of (2S,3S,4S)-4-amino-2,3-epoxy-1-alkanols 4 with diastereoselectivities of up to 95:5.