189264-47-9

Usage

Uses

Used in Fragrance Industry:
3,3a,7,7aα-Tetrahydro-3aα-hydroxy-2H-6-benzofuranone is used as a fragrance ingredient for its ability to add a warm, sweet scent to perfumes, lotions, and air fresheners. Its vanilla-like aroma enhances the overall sensory experience of these products, making them more appealing to consumers.
Used in Food Industry:
In the food industry, 3,3a,7,7aα-Tetrahydro-3aα-hydroxy-2H-6-benzofuranone is used as a flavoring agent, particularly in baked goods and desserts. Its sweet, vanilla-like flavor profile complements the taste of these food products, enhancing their overall flavor and making them more enjoyable for consumers.
If there are additional applications or industries where 3,3a,7,7aα-Tetrahydro-3aα-hydroxy-2H-6-benzofuranone is used, they can be listed as follows:
Used in [Additional Application Industry]:
3,3a,7,7aα-Tetrahydro-3aα-hydroxy-2H-6-benzofuranone is used as [application type] for [application reason].

Upstream product

• 189264-45-7 cleroindicin D 
• 443923-77-1 (2R,3R)-8-(2-hydroxy)ethyl-2,3-diphenyl-1,4-dioxaspiro[4.5]deca-6,9-dien-8-ol 
• 443095-50-9 ethyl 2-[(2R,3R)-8-hydroxy-2,3-diphenyl-1,4-dioxaspiro[4.5]deca-6,9-dien-8-yl]acetate 

Downstream Products

• 189264-44-6 cleroindicin C 

Relevant academic research and scientific papers

Catalytic enantioselective silylation of acyclic and cyclic triols: Application to total syntheses of cleroindicins D, F, and C

(Chemical Equation Presented) Pick one out of three: Acyclic and cyclic 1,2,3-triols are silylated with exceptional site- and enantioselectivity by a small-molecule catalyst to afford silyl ethers having a neighboring diol moiety. The new process is appli

From p-benzoquinone to cyclohexane chirons: First asymmetric synthesis of (+)-rengyolone and (+)- and (-)-menisdaurilide

Starting from a common, easily available, enantiopure monoketal of p-benzoquinone, the synthesis of a large number of cyclohexane chirons has been achieved. The first synthesis of (+)-rengyolone and (+)- and (-)-menisdaurilide has been performed from one of these new building blocks. The wide variety of functional groups of this series of chirons makes them useful for subsequent synthetic processes.

First synthesis of (+)-rengyolone and (+)- and (-)-menisdaurilide

The benzofuranone natural products (+)-rengyolone and (+)- and (-)-menisdaurilide have been synthesised for the first time from a common enantiopure cyclohexane building block derived from a monoketal of p-benzoquinone.