182699-79-2

Basic information

• Product Name: (+)-(3aR,3aS,7aR)-3a,4,5,7a-tetrahydro-3,6-dimethylbenzofuran-2(3H)-one
• Synonyms: (+)-(3aR,3aS,7aR)-3a,4,5,7a-tetrahydro-3,6-dimethylbenzofuran-2(3H)-one
• CAS NO: 182699-79-2
• Molecular Weight: 166.22
• Mol File: 182699-79-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (+)-(3aR,3aS,7aR)-3a,4,5,7a-tetrahydro-3,6-dimethylbenzofuran-2(3H)-one(CAS DataBase Reference)
• NIST Chemistry Reference: (+)-(3aR,3aS,7aR)-3a,4,5,7a-tetrahydro-3,6-dimethylbenzofuran-2(3H)-one(182699-79-2)
• EPA Substance Registry System: (+)-(3aR,3aS,7aR)-3a,4,5,7a-tetrahydro-3,6-dimethylbenzofuran-2(3H)-one(182699-79-2)

Safety Data

• Hazardous Substances Data: 182699-79-2(Hazardous Substances Data)

Upstream product

• 263163-03-7 (+)-(3aS,7aR)-2,3,3a,4,5,7a-hexahydro-6-methylbenzofuran-2(3H)-one 
• 591-24-2 3-Methylcyclohexanone 
• 20778-34-1 2-(4-methyl-2-oxocyclohex-3-en-1-yl)acetic acid 
• 287720-48-3 (2RS)-2-<(1R)-4-methylcyclohex-3-enyl>propanoic acid 
• 477717-60-5 (3aS,7aS)-6-methyl-3-methylene-3a,4,5,7a-tetrahydrobenzofuran-2(3H)-one 

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

131. Determination of the configuration of wine lactone

The intense sweet and coconut-like smelling odorant 1, named 'wine lactone', was isolated from different wine varieties. The chemical structure of this compound, which has not yet been detected in wine or a food, was identified by high-resolution mass spe