858132-52-2

Basic information

• Product Name: (1R,2S,3R)-1,3-diacetoxy-2-methyl-1-phenylbutan
• Synonyms: (1R,2S,3R)-1,3-diacetoxy-2-methyl-1-phenylbutan
• CAS NO: 858132-52-2
• Molecular Weight: 264.321
• Mol File: 858132-52-2.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: (1R,2S,3R)-1,3-diacetoxy-2-methyl-1-phenylbutan(CAS DataBase Reference)
• NIST Chemistry Reference: (1R,2S,3R)-1,3-diacetoxy-2-methyl-1-phenylbutan(858132-52-2)
• EPA Substance Registry System: (1R,2S,3R)-1,3-diacetoxy-2-methyl-1-phenylbutan(858132-52-2)

Safety Data

• Hazardous Substances Data: 858132-52-2(Hazardous Substances Data)

Upstream product

• 93-55-0 1-phenyl-propan-1-one 
• 6668-24-2 2-methyl-1-phenyl-1,3-butanedione 
• 902451-93-8 (4R,5S)-2-(4-Methoxy-phenyl)-5-methyl-4-phenyl-[1,3]dioxane 
• 283151-88-2 [3R,4R]-(+)-4-hydroxy-3-methyl-4-phenyl-2-butanone 
• 16735-22-1 (S)-3-hydroxy-2-methyl-1-phenylpropan-1-one 
• 942150-89-2 (2R,4R,5S)-2-(4-methoxyphenyl)-5-methyl-4-phenyl[1,3]dioxane 
• 902451-78-9 (S)-3-(4-methoxybenzyloxy)-2-methyl-1-phenylpropan-1-one 
• 902451-82-5 (2S,3R)-3-(4-methoxybenzyloxy)-2-methyl-3-phenylpropan-1-ol 
• 902451-88-1 (3R,4R)-4-(4-methoxybenzyloxy)-3-methyl-4-phenylbutan-2-one 
• 902451-86-9 (3S,4R)-4-(4-methoxybenzyloxy)-3-methyl-4-phenylbutan-2-ol 
• 902451-84-7 (2R,3R)-3-(4-methoxybenzyloxy)-2-methyl-3-phenylpropan-1-al 
• 108-24-7 acetic anhydride 
• 902451-80-3 (1R,2S)-3-(4-methoxybenzyloxy)-2-methyl-1-phenylpropan-1-ol 

Downstream Products

• 1027139-76-9 C₂₃H₃₁NO₁₀ 

Relevant articles and documents

A concise synthesis of (+)-conagenin and its isomer using chiral tricyclic iminolactones

An efficient synthesis of (+)-conagenin, a novel immunomodulator produced by Streptomyces roseosporus, has been achieved via the shortest route at present. At the same time, 2-epiconagenin was synthesized according to the same methodology.

Stereoselective synthesis of an immunomodulator (+)-conagenin using dirhodium(II)-catalyzed C-H amination and chelation-controlled reductions as key steps

Stereoselective synthesis of an immunomodulator (+)-conagenin from commercially available optically active methyl 3-hydroxy-2-methylpropanoate was achieved using dirhodium(II)-catalyzed C-H amination and chelation-controlled reductions as key steps. Georg