133472-83-0

Basic information

• Product Name: 4,4-bis[4-(benzyloxy)phenyl]pentanol
• Synonyms: 4,4-bis[4-(benzyloxy)phenyl]pentanol
• CAS NO: 133472-83-0
• Molecular Weight: 452.593
• Mol File: 133472-83-0.mol

Chemical Properties

• CAS DataBase Reference: 4,4-bis[4-(benzyloxy)phenyl]pentanol(CAS DataBase Reference)
• NIST Chemistry Reference: 4,4-bis[4-(benzyloxy)phenyl]pentanol(133472-83-0)
• EPA Substance Registry System: 4,4-bis[4-(benzyloxy)phenyl]pentanol(133472-83-0)

Safety Data

• Hazardous Substances Data: 133472-83-0(Hazardous Substances Data)

Upstream product

• 100-39-0 benzyl bromide 
• 100-44-7 benzyl chloride 
• 126-00-1 4,4-bis(4-hydroxyphenyl)valeric acid 
• 184866-14-6 benzyl 4,4-bis[4-(benzyloxy)phenyl]pentanoate 
• 25051-22-3 4,4-bis<4'-(benzyloxy)phenyl>valeric acid 

Downstream Products

• 133472-84-1 -Br 
• 184866-16-8 Methanesulfonic acid 4,4-bis-(4-benzyloxy-phenyl)-pentyl ester 
• 184866-22-6 Dimethyl-thiocarbamic acid S-(4-{[4,4-bis-(4-benzyloxy-phenyl)-pentyl]-methyl-carbamoyl}-phenyl) ester 
• 184866-25-9 N-[4,4-Bis-(4-benzyloxy-phenyl)-pentyl]-4-mercapto-N-methyl-benzamide 
• 184866-19-1 [4,4-Bis-(4-benzyloxy-phenyl)-pentyl]-methyl-amine 
• 133472-85-2 -OH 

Relevant articles and documents

Salidroside analog (4,4-di-(4-hydroxyphenyl)amyl-beta-D-glucopyranoside) and synthesis method thereof

The invention belongs to the field of catalytic synthesis, and particularly relates to salidroside analog (4,4-di-(4-hydroxyphenyl)amyl-beta-D-glucopyranoside) and a preparation method thereof. The structural formula of the 4,4-di-(4-hydroxyphenyl)amyl-be

Synthesis of a series of focally-substituted organothiol dendrons

The synthesis of new organothiol-functionalized dendrons of generation 1-4 is described. Several modifications to the original method for preparation of dendrons are detailed that were found to improve the yield and aid in scale-up. A particularly advanta

Hyperbranched Macromolecules via a Novel Double-Stage Convergent Growth Approach

A novel double-stage convergent growth approach for the preparation of dendritic macromolecules is described. In the first stage, convergent growth with 4,4-bis(4′-hydroxyphenyl)pentanol as the building block is used to create symmetrical dendritic struct