54154-69-7

Basic information

• Product Name: rac-(3aS,9bR)-3a,4,5,9b-tetrahydronaphtho<1,2-b>furan-2(3H)-one
• CAS NO: 54154-69-7
• Molecular Weight: 188.226
• Mol File: 54154-69-7.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: rac-(3aS,9bR)-3a,4,5,9b-tetrahydronaphtho<1,2-b>furan-2(3H)-one(CAS DataBase Reference)
• NIST Chemistry Reference: rac-(3aS,9bR)-3a,4,5,9b-tetrahydronaphtho<1,2-b>furan-2(3H)-one(54154-69-7)
• EPA Substance Registry System: rac-(3aS,9bR)-3a,4,5,9b-tetrahydronaphtho<1,2-b>furan-2(3H)-one(54154-69-7)

Safety Data

• Hazardous Substances Data: 54154-69-7(Hazardous Substances Data)

Upstream product

• 529-34-0 3,4-dihydronaphthalene-1(2H)-one 
• 123990-74-9 β-Carbethoxy-β-carbethoxymethyl-α-tetralone 
• 6742-31-0 1,2,3,4-tetrahydro-1-oxo-2-naphthaleneacetic acid 
• 6742-26-3 2-ethoxycarbonyl-1-tetralone 
• 105207-09-8 α-Tetralol-β-acetic acid 
• 101640-55-5 But-3-enoic acid bicyclo[4.2.0]octa-1,3,5-trien-7-yl ester 

Relevant articles and documents

Multiple Absolute Stereocontrol in Cascade Lactone Formation via Dynamic Kinetic Resolution Driven by the Asymmetric Transfer Hydrogenation of Keto Acids with Oxo-Tethered Ruthenium Catalysts

A straightforward asymmetric construction of chiral fused γ- and δ-lactones containing multiple contiguous stereocenters was successfully developed by either (1) the dynamic kinetic resolution-asymmetric transfer hydrogenation (DKR-ATH) reaction using oxo

A Simple Synthesis of α-Tetralol-β-acetic Acid and β-Propionic Acid cis-Lactones

A short and convenient synthesis of α-tetralone β-acetic acid and α-tetralone-β-propionic acid starting from tetralone and facile formation of only cis-lactones by NaBH4/H+ are described.