69222-28-2

Basic information

• Product Name: (1aS,2S,3R,7bR)-1a,2,3,7b-tetrahydronaphtho[1,2-b]oxirene-2,3-diol
• Synonyms: Naphth[1,2-b]oxirene-2,3-diol, 1a,2,3,7b-tetrahydro-, (1aR,2R,3S,7bS)-rel-
• CAS NO: 69222-28-2
• Molecular Formula: C₁₀H₁₀O₃
• Molecular Weight: 178.1846
• Mol File: 69222-28-2.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 382.5°C at 760 mmHg
• Flash Point: 185.1°C
• Density: 1.484g/cm³
• Vapor Pressure: 1.56E-06mmHg at 25°C
• Refractive Index: 1.689
• CAS DataBase Reference: (1aS,2S,3R,7bR)-1a,2,3,7b-tetrahydronaphtho[1,2-b]oxirene-2,3-diol(CAS DataBase Reference)
• NIST Chemistry Reference: (1aS,2S,3R,7bR)-1a,2,3,7b-tetrahydronaphtho[1,2-b]oxirene-2,3-diol(69222-28-2)
• EPA Substance Registry System: (1aS,2S,3R,7bR)-1a,2,3,7b-tetrahydronaphtho[1,2-b]oxirene-2,3-diol(69222-28-2)

Safety Data

• Hazardous Substances Data: 69222-28-2(Hazardous Substances Data)

Upstream product

• 771-16-4 (+/-)-trans-1,2-dihydroxy-1,2-dihydronaphthalene 

Relevant articles and documents

Chemistry of anti- and syn-1,2:3,4-Naphthalene Dioxides and Their Potential Relevance as Metabolic Intermediates

The reactivity, site of attack, and stereochemistry of reactions of a variety of nucleophiles with the anti- and syn-1,2:3,4-naphthalene dioxides have been explored.In most cases, substituted tetrahydronaphthalene products arising through attack at the C-1 and C-4 positions in the anti mode were obtained.These isomeric dioxides provide excellent precursors for a number of difficultly accessible 1,4-disubstituted naphthalene derivatives such as 1,4-diphenoxynaphthalene and 1,4-dicyanonaphthalene.Evidence is also presented that anti-naphthalene dioxide constitutes an intermediate metabolite in the rat.