908588-41-0

Basic information

• Product Name: (R)-5-(2,5-dihydroxyphenyl)-3-(4-methylpent-3-en-1-yl)furan-2(5H)-one
• Synonyms: (R)-5-(2,5-dihydroxyphenyl)-3-(4-methylpent-3-en-1-yl)furan-2(5H)-one
• CAS NO: 908588-41-0
• Molecular Weight: 274.317
• Mol File: 908588-41-0.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (R)-5-(2,5-dihydroxyphenyl)-3-(4-methylpent-3-en-1-yl)furan-2(5H)-one(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-5-(2,5-dihydroxyphenyl)-3-(4-methylpent-3-en-1-yl)furan-2(5H)-one(908588-41-0)
• EPA Substance Registry System: (R)-5-(2,5-dihydroxyphenyl)-3-(4-methylpent-3-en-1-yl)furan-2(5H)-one(908588-41-0)

Safety Data

• Hazardous Substances Data: 908588-41-0(Hazardous Substances Data)

Upstream product

• 1580541-84-9 (R)-5-[2',5'-bis(methoxymethoxyphenyl)]-3-(4''-methylnona-3''-en-1''-yl)-2(5H)-furanone 
• 1580541-82-7 (R)-[2,5-bis(methoxymethoxy)phenyl]prop-2-en-1-yl 6-methyl-2-methylidenehept-5-enoate 
• 1580541-80-5 6-dimethyl-2-methylidenehept-5-enoic acid 
• 1580541-74-7 (R)-1-[2',5'-bis(methoxymethoxy)phenyl]prop-2-en-1-ol 
• 1580541-73-6 (2'R,3'S)-2-{3'-[2'',5''-bis(methoxymethoxy)phenyl]-2',3'-dihydroxyprop-2-enylsulfonyl}-1,3-benzothiazole 
• 1580541-71-4 (E)-2-{3'-[2'',5''-bis(methoxymethoxy)phenyl]prop-2-enylthio}-1,3-benzothiazole 
• 1580541-70-3 (E)-3-[2,5-bis(methoxymethoxy)phenyl]prop-2-en-1-ol 
• 40931-14-4 ethyl (E)-3-[2,5-bis(methoxymethoxy)phenyl]prop-2-enoate 
• 13709-07-4 2,5-bis(methoxymethoxy)benzaldehyde 
• 1194-98-5 2,5-Dihydroxybenzaldehyde 

Relevant articles and documents

Concise syntheses and biological activities of ganomycin I and fornicin A

The first enantioselective syntheses of ganomycin I, a meroterpenoid isolated from the Vietnamese mushroom Ganoderma colossum, and the related meroterpenoid fornicin A were accomplished. Our methodology for the total syntheses of these compounds featured the construction of the butenolide moiety by asymmetric dihydroxylation followed by Julia-Kocienski type olefin formation and ring-closing metathesis reactions. The absolute configurations of the two natural products were determined by comparisons of specific rotation. A cell-based assay of the synthetic compounds with transfected human embryonic kidney 293 tetoff (E-PR293) cells indicated that ganomycin I possesses cytotoxicity and fornicin A possesses weak anti-HIV-1 protease activity without cytotoxicity.