37669-01-5

Basic information

• Product Name: 2,3-O-isopropylideneerythrose
• Synonyms: 2,3-O-isopropylideneerythrose
• CAS NO: 37669-01-5
• Molecular Formula: C7H12O4
• Molecular Weight: 160.17
• Mol File: 37669-01-5.mol
• Article Data: 3

Chemical Properties

• Melting Point: 29-31 °C
• Boiling Point: 249.1°C at 760 mmHg
• Flash Point: 99.2°C
• Appearance: /
• Density: 1.192g/cm³
• Vapor Pressure: 0.00375mmHg at 25°C
• Refractive Index: 1.495
• PKA: 14.20±0.10(Predicted)
• CAS DataBase Reference: 2,3-O-isopropylideneerythrose(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3-O-isopropylideneerythrose(37669-01-5)
• EPA Substance Registry System: 2,3-O-isopropylideneerythrose(37669-01-5)

Safety Data

• Hazardous Substances Data: 37669-01-5(Hazardous Substances Data)

Usage

InChI:InChI=1/C7H12O4/c1-7(2)10-5(3-8)6(4-9)11-7/h3,5-6,9H,4H2,1-2H3/t5-,6+/m1/s1

Upstream product

• 127743-12-8 [(4S,5R)-2,2-Dimethyl-5-((E)-styryl)-[1,3]dioxolan-4-yl]-methanol 
• 58645-35-5 3,4-O-isopropylidine L-arabinopyranose 

Downstream Products

• 114817-96-8 (4S,5R)-2,2-dimethyl-4-hydroxymethyl-5-vinyl-1,3-dioxolane 
• 120142-89-4 2,3-O-isopropylidene-β-L-erythrofuranosyl 2,3-O-isopropylidene-β-L-erythrofuranoside 

Relevant articles and documents

Chiron Approaches to the Antitumor Natural Product Fuzanin D

Fuzanin D, a pyridine-containing natural product, which exhibits cytotoxic activity against DLD-1 cells, is synthesized in a concise manner using l-arabinose or ethyl l-lactate as chiral pool substrates in nine steps (14.4% overall yield) and six steps (30.8% overall yield), respectively. The key steps involve Wittig olefination and olefin cross--metathesis.

Total synthesis of (+)-altholactone

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