358349-92-5

Basic information

• Product Name: (4-phenoxybutyl)benzene
• Synonyms: (4-phenoxybutyl)benzene
• CAS NO: 358349-92-5
• Molecular Weight: 226.318
• Mol File: 358349-92-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (4-phenoxybutyl)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: (4-phenoxybutyl)benzene(358349-92-5)
• EPA Substance Registry System: (4-phenoxybutyl)benzene(358349-92-5)

Safety Data

• Hazardous Substances Data: 358349-92-5(Hazardous Substances Data)

Upstream product

• 4830-93-7 1-Chloro-4-phenylbutane 
• 139-02-6 sodium phenoxide 
• 64-17-5 ethanol 
• 872275-23-5 5-phenoxy-2-phenyl-valeronitrile 
• 108-88-3 toluene 
• 3360-41-6 4-phenyl-butan-1-ol 
• 108-95-2 phenol 
• 19790-62-6 4-phenoxybutyraldehyde 
• 13633-25-5 1-Bromo-4-phenylbutane 
• 1200-03-9 4-bromophenyl butyl ether 
• 100-58-3 phenylmagnesium bromide 

Relevant articles and documents

Chemoselective Deoxygenation of 2° Benzylic Alcohols through a Sequence of Formylation and B(C6F5)3-Catalyzed Reduction

A sequence of formylation and B(C6F5)3-catalyzed reduction of the resulting formate with Et3SiH enables the chemoselective deoxygenation of secondary benzylic alcohols. Primary benzylic and tertiary non-benzylic alcohols are not reduced by this protocol. The formyl group fulfills a double role as activator and self-sacrificing protecting group. The deoxygenation of these formates is fast and can be carried out in the presence of other potentially reducible groups. Neighboring-group participation was found in the deoxygenation of certain diol motifs.

METHODS AND COMPOSITIONS FOR MODULATING SPHINGOSINE-1-PHOSPHATE (S1P) RECEPTOR ACTIVITY

The present invention relates to compounds which modulate the activity of the SI P1 receptor, the use of these compounds for treating conditions associated with signaling through the S1 P1 receptor, and pharmaceutical compositions comprising these compounds.