35185-96-7

Basic information

• Product Name: 1,4-EPOXY-1,2,3,4-TETRAHYDRONAPHTHALENE
• Synonyms: 1,2,3,4-Tetrahydronaphthalene 1,4-endoxide;1,2,3,4-Tetrahydronaphthalene-1,4-endo-oxide;1,4-EPOXY-1,2,3,4-TETRAHYDRONAPHTHALENE;1,4-EPOXY-1,2,3,4-TETRAHYDRONAPHTHALENE 98%;1,4-Epoxy-1,2,3,4-tetrahydronaphthalene,98%
• CAS NO: 35185-96-7
• Molecular Formula: C₁₀H₁₀O
• Molecular Weight: 146.19
• Mol File: 35185-96-7.mol
• Article Data: 1

Chemical Properties

• Melting Point: 14.5°C
• Boiling Point: 225.81°C (rough estimate)
• Flash Point: 90 °C
• Appearance: /
• Density: 1.0900
• Vapor Pressure: 0.657mmHg at 25°C
• Refractive Index: 1.5540 (estimate)
• CAS DataBase Reference: 1,4-EPOXY-1,2,3,4-TETRAHYDRONAPHTHALENE(CAS DataBase Reference)
• NIST Chemistry Reference: 1,4-EPOXY-1,2,3,4-TETRAHYDRONAPHTHALENE(35185-96-7)
• EPA Substance Registry System: 1,4-EPOXY-1,2,3,4-TETRAHYDRONAPHTHALENE(35185-96-7)

Safety Data

• Hazardous Substances Data: 35185-96-7(Hazardous Substances Data)

Usage

Chemical Properties

CLEAR COLOURLESS LIQUID

InChI:InChI=1/C10H10O/c1-2-4-8-7(3-1)9-5-6-10(8)11-9/h1-4,9-10H,5-6H2

Upstream product

• 75802-19-6 1-Ethoxy-1,3-dihydroisobenzofuran 

Downstream Products

• 76561-85-8 (1RS,2RS,3SR,4SR)?1,2,3,4?tetrahydronaphthalene?1,2,3,4?tetraol 
• 1031335-20-2 (4-hydroxy-1,2,3,4-tetrahydro-naphthalen-1-yl)-(3-trifluoromethoxy-benzyl)-amine 
• 91-20-3 naphthalene 
• 1009631-96-2 1,4-diallyl-1,2,3,4-tetrahydronaphthalene 
• 1009632-14-7 C₁₉H₁₈ 
• 529-33-9 1,2,3,4-Tetrahydro-1-naphthol 

Relevant articles and documents

7-Oxabicyclohept-2-ene and Related Materials by Reductive Elimination

The cycloadduct 1 of furan and (E)-1,2-bis(phenylsulfonyl)ethylene has been converted to various derivatives which in turn have been subjected to sodium amalgam reductive elimination conditions.Some of these procedures constitute useful methods for the preparation of the title olefin.The amalgam reduction of 1 provides modest yields of 7-oxabicyclohepta-2,5-diene.The cycloadduct of isobenzofuran and the reactive dienophile was prepared and subjected to analogous reactions.Various reaction steps which compete with reductive elimination have been identified.