1016544-88-9

Basic information

• Product Name: (4-bromophenyl)(3,4,5-trimethoxyphenyl)methanol
• Synonyms: (4-bromophenyl)(3,4,5-trimethoxyphenyl)methanol
• CAS NO: 1016544-88-9
• Molecular Weight: 353.213
• Mol File: 1016544-88-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (4-bromophenyl)(3,4,5-trimethoxyphenyl)methanol(CAS DataBase Reference)
• NIST Chemistry Reference: (4-bromophenyl)(3,4,5-trimethoxyphenyl)methanol(1016544-88-9)
• EPA Substance Registry System: (4-bromophenyl)(3,4,5-trimethoxyphenyl)methanol(1016544-88-9)

Safety Data

• Hazardous Substances Data: 1016544-88-9(Hazardous Substances Data)

Upstream product

• 589-87-7 1,4-bromoiodobenzene 
• 86-81-7 3,4,5-trimethoxy-benzaldehyde 
• 133095-91-7 3,4,5-trimethoxyphenylmagnesium bromide 
• 1122-91-4 4-bromo-benzaldehyde 

Downstream Products

• 1016544-89-0 (4-bromophenyl)(3,4,5-trimethoxyphenyl)methanone 
• 1392140-06-5 4'-bromo-3,4,5-trimethoxybenzophenone dimethyl acetal 
• 1392140-02-1 4'-(dihydroxylboryl)-3,4,5-trimethoxybenzophenone 

Relevant articles and documents

Synthesis and biological evaluation of boronic acid-containing phenstatin analogues

A series of boronic acid-containing benzophenones was synthesized by introducing a boronic acid as an acceptor-type functional group into the aromatic ring B of the phenstatin skeleton. Among the compounds synthesized, 4c in which a hydroxyl group on the

BENZOPHENONE DERIVATIVES USEFUL FOR INHIBITING FORMATION OF MICROTUBULE

Disclosed herein are novel benzophenone derivatives represented by formula I, a pharmaceutically acceptable salt thereof, a hydrate thereof or a solvate thereof, a pharmacological composition containing the same, and a use of the composition as therapeutic drugs. The benzophenone derivatives have an inhibition activity of microtubule formation and can be used to treat a normal proliferative state of a malignant tumor by killing the actively proliferating cells.