250369-59-6

Basic information

• Product Name: (3aR,4R,5S,6aR)-5-Acetyl-4-benzyloxy-tetrahydro-furo[2,3-b]furan-2-one
• Synonyms: (3aR,4R,5S,6aR)-5-Acetyl-4-benzyloxy-tetrahydro-furo[2,3-b]furan-2-one
• CAS NO: 250369-59-6
• Molecular Weight: 276.289
• Mol File: 250369-59-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (3aR,4R,5S,6aR)-5-Acetyl-4-benzyloxy-tetrahydro-furo[2,3-b]furan-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: (3aR,4R,5S,6aR)-5-Acetyl-4-benzyloxy-tetrahydro-furo[2,3-b]furan-2-one(250369-59-6)
• EPA Substance Registry System: (3aR,4R,5S,6aR)-5-Acetyl-4-benzyloxy-tetrahydro-furo[2,3-b]furan-2-one(250369-59-6)

Safety Data

• Hazardous Substances Data: 250369-59-6(Hazardous Substances Data)

Upstream product

• 14131-84-1 2,3:5,6-di-O-isopropylidene-α-D-mannofuranose 
• 79241-07-9 (R)-4-((2S,3R)-3-(benzyloxy)-2,3-dihydrofuran-2-yl)-2,2-dimethyl-1,3-dioxolan 
• 17087-84-2 (3aS,4R,6R,6aS)-4-chloro-6-((R)-2,2-dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxole 
• 68144-11-6 1,4-anhydro-2-deoxy-5,6-O-isopropylidene-D-arabinohex-1-enitol 
• 530-26-7 D-Mannose 
• 250369-64-3 C₁₉H₂₈O₇ 
• 250369-66-5 [4-benzyloxy-2-ethoxy-5-(1-hydroxy-ethyl)-tetrahydro-furan-3-yl]-acetic acid ethyl ester 
• 250369-67-6 (5-acetyl-4-benzyloxy-2-ethoxy-tetrahydro-furan-3-yl)-acetic acid ethyl ester 

Relevant articles and documents

Synthesis of Fused Tetrahydrofuran-γ-lactone Motifs via One-Pot Ring Expansion of Cyclopropane Rings

An efficient method for constructing fused tetrahydrofuran-γ-lactone scaffolds, such as 8, is presented. Key to this strategy is an acid-catalyzed ring expansion of cyclopropyl precursor 6 that proceeds in the presence of MeSO3H in acetone and produces th

Synthetic studies on norrisolide: Enantioselective synthesis of the norrisane side chain

Norrisolide (1) belongs to a family of marine diterpenes that are characterized by the assembly of a bicyclic core with a unique and highly oxygenated side chain (norrisane side chain). As a prelude to the synthesis of 1, we present herein a short, effici