90847-51-1

Basic information

• Product Name: 4-aminobutane-1,2,3-triol
• Synonyms: 4-aminobutane-1,2,3-triol;4-Amino-1,2,3-butanetriol
• CAS NO: 90847-51-1
• Molecular Formula: C₄H₁₁NO₃
• Molecular Weight: 121.13504
• EINECS: 292-681-8
• Mol File: 90847-51-1.mol

Chemical Properties

• Boiling Point: 357°Cat760mmHg
• Flash Point: 169.7°C
• Appearance: /
• Density: 1.323g/cm³
• Vapor Pressure: 1.57E-06mmHg at 25°C
• Refractive Index: 1.538
• CAS DataBase Reference: 4-aminobutane-1,2,3-triol(CAS DataBase Reference)
• NIST Chemistry Reference: 4-aminobutane-1,2,3-triol(90847-51-1)
• EPA Substance Registry System: 4-aminobutane-1,2,3-triol(90847-51-1)

Safety Data

• Hazardous Substances Data: 90847-51-1(Hazardous Substances Data)

Usage

InChI:InChI=1/C4H11NO3/c5-1-3(7)4(8)2-6/h3-4,6-8H,1-2,5H2

Upstream product

• 131507-69-2 Benzyl r-3-<<(tert-Butyl)dimethylsilyl>oxy>-t-4,t-5-dihydroxy-1,2-oxazinane-2-carboxylate 

Downstream Products

• 1118720-72-1 C₇₀H₈₇N₇O₂₀ 

Relevant articles and documents

From 1-(Silyloxy)butadiene to 4-Amino-4-deoxy-DL-erythrose and to 1-Amino-1-deoxy-DL-erythriol Derivatives via hetero-Diels-Alder Reactions with Acylnitroso Dienophiles

Acylnitroso dienophiles 4 reacted instantly with 1-(silyloxy)butadiene 5α and led in good yield to the regioisomeric cycloadducts 6 (major) and 7 (minor; Scheme 2, Table 1). cis-Hydroxylation of these primary cycloadducts with OsO4 (catalyst) occurred stereospecifically and in high yield (-> 8 and 9, resp.: Scheme 2).It was followed by reductive ring cleavage to give either 1-amino-1-deoxy-DL-erythriol or 4-amino-4-deoxy-DL-erythrose derivatives 10 and 14, respectively, depending on the nature of the reducing agent (Schemes 3 and 4).