17684-73-0

Basic information

• Product Name: 5-phenylbicyclo[1.1.1]pentan-5-ol
• Synonyms: 5-phenylbicyclo[1.1.1]pentan-5-ol
• CAS NO: 17684-73-0
• Molecular Formula: C₁₁H₁₂O
• Molecular Weight: 160.21
• Mol File: 17684-73-0.mol

Chemical Properties

• Boiling Point: 280.5°Cat760mmHg
• Flash Point: 101.8°C
• Appearance: /
• Density: 1.238g/cm³
• Vapor Pressure: 0.0018mmHg at 25°C
• Refractive Index: 1.647
• CAS DataBase Reference: 5-phenylbicyclo[1.1.1]pentan-5-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 5-phenylbicyclo[1.1.1]pentan-5-ol(17684-73-0)
• EPA Substance Registry System: 5-phenylbicyclo[1.1.1]pentan-5-ol(17684-73-0)

Safety Data

• Hazardous Substances Data: 17684-73-0(Hazardous Substances Data)

Usage

InChI:InChI=1/C11H12O/c12-11(9-6-10(11)7-9)8-4-2-1-3-5-8/h1-5,9-10,12H,6-7H2

Upstream product

• 5407-98-7 1-cyclobutyl-1-phenyl-methanone 

Downstream Products

• 3721-95-7 Cyclobutanecarboxylic acid 
• 5407-98-7 1-cyclobutyl-1-phenyl-methanone 
• 93061-30-4 bicyclo<1.1.1>pentanone 
• 93039-41-9 3-oxocyclobutyl phenyl ketone 
• 65-85-0 benzoic acid 
• 27856-20-8 1-hydroxy-3-phenylcyclopent-3-ene 
• 29586-29-6 1-acetoxy-3-phenyl-3-cyclopentene 
• 148749-91-1 2-Phenylbicyclo<1.1.1>pentane 
• 148749-94-4 2-Benzoylbicyclo<1.1.1>pentane 
• 64145-51-3 3-phenylcyclopentanone 
• 148749-90-0 2-phenylbicyclo[1.1.1]pentan-2-yl acetate 

Relevant articles and documents

SUBSTITUTED DIAMINOCARBOXAMIDE AND DIAMINOCARBONITRILE PYRIMIDINES, COMPOSITIONS THEREOF, AND METHODS OF TREATMENT THEREWITH

Provided herein are Diaminopyrimidine Compounds having the following structures: wherein R1, R2, R3, and R4 are as defined herein, compositions comprising an effective amount of a Diaminopyrimidine Compound, and methods for treating or preventing liver fibrotic disorders or a condition treatable or preventable by inhibition of a JNK pathway.

Bicyclopentanone. Synthesis, Thermal Chemistry, and Photochemistry

Bicyclopentanone (1) has been prepared in two steps, the key reaction being the ozonolysis of 2-phenylbicyclopentan-2-ol (6).On heating, 1 undergoes cycloreversion to allylketene (13).The activation parameters and solvent effects for this process suggest that the reaction is concerted and that the transition state is relatively nonpolar.The predominant photochemical pathway for 1 is decarbonylation to bicyclobutane (16).Cycloreversion to 13 is a minor reaction mode.Both the thermal and photochemical results are rationalized by considering the high strain energy and novel geometrical features of 1, and, in the latter case, the unusually high energy of its 1(n?excit.) state.