1367297-96-8

Basic information

• Product Name: trans-3,5-bis(triphenylmethyloxy)stilbene-4'-O-β-D-glucopyranoside
• Synonyms: trans-3,5-bis(triphenylmethyloxy)stilbene-4'-O-β-D-glucopyranoside
• CAS NO: 1367297-96-8
• Molecular Weight: 875.03
• Mol File: 1367297-96-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: trans-3,5-bis(triphenylmethyloxy)stilbene-4'-O-β-D-glucopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: trans-3,5-bis(triphenylmethyloxy)stilbene-4'-O-β-D-glucopyranoside(1367297-96-8)
• EPA Substance Registry System: trans-3,5-bis(triphenylmethyloxy)stilbene-4'-O-β-D-glucopyranoside(1367297-96-8)

Safety Data

• Hazardous Substances Data: 1367297-96-8(Hazardous Substances Data)

Upstream product

• 38963-95-0 trans-resveratroloside 
• 76-83-5 trityl chloride 

Relevant articles and documents

Reaction of several resveratrol glycoside derivatives with hypochlorites in various media

The reactions of pterostilbenoside (trans-3,5-dimethoxystilben-4′-O- β-D-glucoside) and Ar-O-Tr derivatives of resveratroloside (3,5-dihydroxystilben-4′-O-β-D-glucoside) and pinostilbenoside (3-methoxy-5-hydroxystilben-4′-O-β-D-glucoside) with NaOCl and t-BuOCl in the presence of the stable nitroxyl radical TEMPO were studied in various media. It was found that the principal product of pterostilbenoside transformation was its 2,6-dichloroderivative, a part of which was oxidized to form 2,6-dichloropterostilbene glucuronide. Trityl ethers of resveratroloside and pinostilbenoside reacted with the hypochlorites to form mixtures of products.