6143-30-2

Basic information

• Product Name: 5-NORBORNENE-2-PHENYL
• Synonyms: 5-NORBORNENE-2-PHENYL;5-PHENYLBICYCLO[2.2.1]-2-HEPTENE;5-Phenylbicyclo[2.2.1]hept-2-ene;5-Phenylnorbornene;Bicyclo[2.2.1]hept-2-ene,5-phenyl-
• CAS NO: 6143-30-2
• Molecular Formula: C₁₃H₁₄
• Molecular Weight: 170.25
• Product Categories: Norbornene Derivatives
• Mol File: 6143-30-2.mol
• Article Data: 12

Chemical Properties

• Boiling Point: 70.5-71℃ (0.3 Torr)
• Flash Point: 99.0±10.3℃
• Appearance: /
• Density: 1.046±0.06 g/cm3 (20 ºC 760 Torr)
• Vapor Pressure: 0.038mmHg at 25°C
• Refractive Index: 1.5510 (589.3 nm 20℃)
• CAS DataBase Reference: 5-NORBORNENE-2-PHENYL(CAS DataBase Reference)
• NIST Chemistry Reference: 5-NORBORNENE-2-PHENYL(6143-30-2)
• EPA Substance Registry System: 5-NORBORNENE-2-PHENYL(6143-30-2)

Safety Data

• Hazardous Substances Data: 6143-30-2(Hazardous Substances Data)

Usage

General Description

5-NORBORNENE-2-PHENYL is a chemical compound with the molecular formula C15H18. It is a bicyclic compound that contains a norbornene ring system and a phenyl group. 5-NORBORNENE-2-PHENYL is commonly used in the production of various polymers, resins, and specialty chemicals. It exhibits unique physical and chemical properties that make it suitable for a wide range of applications in the fields of materials science, pharmaceuticals, and industrial chemistry. 5-NORBORNENE-2-PHENYL may also be used as a building block in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Overall, it is an important and versatile compound with diverse uses in the chemical industry.

InChI:InChI=1/C13H14/c1-2-4-11(5-3-1)13-9-10-6-7-12(13)8-10/h1-7,10,12-13H,8-9H2

Upstream product

• 591-50-4 iodobenzene 
• 121-46-0 bicyclo[2.2.1]hepta-2,5-diene 
• 100-42-5 styrene 
• 542-92-7 cyclopenta-1,3-diene 
• 1755-01-7 endo-Dicyclopentadien 
• 77-73-6 bi(cyclopentadiene) 
• 498-66-8 norborn-2-ene 
• 71-43-2 benzene 
• 141831-92-7 C₃₃H₂₄O₄S₂ 
• 141831-77-8 2-benzylidene-dinaphtho<2,1-d:1',2'-f><1,3>dithiepine 
• 141832-07-7 2-benzylidene-dinaphtho<2,1-d:1',2'-f><1,3>dithiepine-S,S'-tetroxide 

Downstream Products

• 17989-94-5 endo-2-phenylbicyclo<2.2.1>heptane 
• 42114-05-6 methyl-(1-phenyl-[2]norbornyl)-ether 
• 92251-47-3 formic acid-(1-phenyl-[2]norbornyl ester) 
• 71173-15-4 acetic acid-(1-phenyl-[2]norbornyl ester) 

Relevant articles and documents

Epoxidation and oxidative dihydroxylation of C10–C13 unsaturated bridged hydrocarbons involving hydrogen peroxide and modified forms of heteromolybdic compounds

Induced oxidation of C10–C13 tricyclic bridged olefins synthesized from C5–C8 cyclodiene hydrocarbons using hydrogen peroxide has been studied. It has been shown that phosphomolybdic heteropoly compounds supported on a finely divided carbon material and additionally modified with HBr and CoCO3 or Gd2O3 exhibit high activity in this reaction. Depending on the conditions of the experiments, the main reaction products are the corresponding oxiranes and diols that retain the structure of the reactant hydrocarbons.

[2+4] Cycloaddition of η6-(styrene)chromium tricarbonyl and conjugated dienes

Cycloaddition of η6-(styrene)chromium tricarbonyl to hexa-2,4-diene or cyclopentadiene afford the Diels-Alder adducts with retention of the Cr(CO)3 group, whereas cyclohexa-1,3-diene undergoes aromatization to give η6-(ben

A highly efficient palladacycle catalyst for hydrophenylation of C-, N-, and O-substituted bicyclic alkenes under aerobic condition

A new phosphine-free palladacycle catalyst 4 was prepared from benzyl oxazoline in high yield and fully characterized. With it as catalyst, hydrophenylation reactions of a wide range of bicyclic alkenes, not only norbomene and norborriadiene but also oxa-