250138-83-1

Basic information

• Product Name: (all-R)-[5'-(5''-Benzyloxymethyltetrahydrofuran-2''-yl)tetrahydrofuran-2'-yl]methanol
• Synonyms: (all-R)-[5'-(5''-Benzyloxymethyltetrahydrofuran-2''-yl)tetrahydrofuran-2'-yl]methanol
• CAS NO: 250138-83-1
• Molecular Weight: 292.375
• Mol File: 250138-83-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (all-R)-[5'-(5''-Benzyloxymethyltetrahydrofuran-2''-yl)tetrahydrofuran-2'-yl]methanol(CAS DataBase Reference)
• NIST Chemistry Reference: (all-R)-[5'-(5''-Benzyloxymethyltetrahydrofuran-2''-yl)tetrahydrofuran-2'-yl]methanol(250138-83-1)
• EPA Substance Registry System: (all-R)-[5'-(5''-Benzyloxymethyltetrahydrofuran-2''-yl)tetrahydrofuran-2'-yl]methanol(250138-83-1)

Safety Data

• Hazardous Substances Data: 250138-83-1(Hazardous Substances Data)

Upstream product

• 100-39-0 benzyl bromide 
• 250138-82-0 (2R,2R',5R, 5R')-5,5'-bis(hydroxymethyl)octahydro-2,2'-bifuran 
• 203715-36-0 (5R,6R)-5,6-dihydroxydeca-1,9-diene 
• 39139-91-8 trans-1,5,9-decatriene 

Downstream Products

• 292820-14-5 Hydroquinone-squamocin D dimethyl ether 
• 292820-19-0 (1R,2'R,5'R,2''R,5''R,1'''R,5'''S)-1-[5'-(5''-(1''',5'''-Di(tert-butyldimethylsilyloxy)undecan-1'''-yl)tetrahydrofuran-2''-yl)tetrahydrofuran-2'-yl]-13-(2'''',3'''',4'''',5''''-tetramethoxy-6''''-methylphenyl)tridecan-1-ol 
• 337954-06-0 (1R,5S,2'R,5'R,2''R,5''R)-1-[5'-(5''-Benzyloxymethyltetrahydrofuran-2''-yl)tetrahydrofuran-2'-yl]-5-(tert-butyldimethylsilyloxy)undecan-1-ol 
• 337954-05-9 (5S,2'R,5'R,2''R,5''R)-1-[5'-(5''-Benzyloxymethyltetrahydrofuran-2''-yl)tetrahydrofuran-2'-yl]-5-(tert-butyldimethylsilyloxy)undecan-1-one 
• 337954-15-1 (1R,5S,2'R,5'R,2''R,5''R)-1-[5'-(5''-Benzyloxymethyltetrahydrofuran-2''-yl)tetrahydrofuran-2'-yl]-1,5-di(tert-butyldimethylsilyloxy)undecane 
• 261617-87-2 (2R,5R,6R,9R,10R)-1-benzyloxy-2,5;6,9-diepoxy-10-tetracosanol 
• 250138-85-3 1-((2R,5R,2'R,5'R)-5'-Benzyloxymethyl-octahydro-[2,2']bifuranyl-5-yl)-pent-4-en-1-one 

Relevant articles and documents

Quinone - Annonaceous acetogenins: Synthesis and complex I inhibition studies of a new class of natural product hybrids

The natural product hybrids quinone-mucocin and quinone- squamocin D were synthesized. In these hybrids, the butenolide unit of the annonaceous acetogenins mucocin and squamocin D is exchanged for the quinone moiety of the natural complex I substrate ubiq

Stereocontrolled construction of the trans tetrahydrofuran units in Annonaceous acetogenins

An efficient synthetic method for the construction of trans- tetrahydrofuran (THF) unit from trans-1,5,9-decatriene was successfully developed by means of Sharpless AD reactions and oxidative cyclizations catalyzed by Co(modp)2 under an oxygen