68592-22-3

Usage

Uses

Used in Fragrance Industry:
(4-hydroxycyclohexyl) acetate is used as a fragrance ingredient for its pleasant, floral scent and compatibility with a range of products. It adds a sweet, fruity aroma to cosmetics, personal care products, and household cleaners, enhancing the overall sensory experience for consumers.
Used in Cosmetics and Personal Care Products:
(4-hydroxycyclohexyl) acetate is used as a fragrance ingredient in cosmetics and personal care products to provide a pleasant and appealing scent. Its floral and fruity aroma can enhance the sensory experience of using these products, making them more enjoyable for consumers.
Used in Household Cleaners:
(4-hydroxycyclohexyl) acetate is used as a fragrance ingredient in household cleaners to add a pleasant scent, making the cleaning experience more enjoyable for users. Its compatibility with various cleaning products allows it to be widely used in the industry.

InChI:InChI=1/C8H14O3/c9-7-3-1-6(2-4-7)5-8(10)11/h6-7,9H,1-5H2,(H,10,11)/t6-,7+

Upstream product

• 52263-23-7 4-oxocyclohexaneacetic acid 
• 99799-09-4 2-(4-hydroxycyclohexyl)acetic acid 
• 4350-84-9 lactone de l'acide(hydroxy-4 cyclohexyl)acetique 

Relevant academic research and scientific papers

CARBAMOYL COMPOUNDS AS DGAT1 INHIBITORS 190

DGAT-1 inhibitor compounds of formula (I), pharmaceutically-acceptable salts and pro- drugs thereof are described, together with pharmaceutical compositions, processes for making them and their use in treating, for example, obesity wherein, for example, Ring A is optionally substituted 2,6-pyrazindiyl; X is =O; Ring B is optionally substituted 1,4-phenylene; Y1 is a direct bond or -O-; Y2 is -(CH 2) r- wherein r is 2 or 3; n is 0 or n is 1 when Y1 is a direct bond between Ring B and Ring C and when Ring B is 1,4-phenylene and Ring C is (4-6C)cycloalkane; Ring C is optionally substituted (4-6C)cycloalkane, (7-10C)bicycloalkane, (8-12C)tricycloalkane, phenylene or pryidindiyl; L is a direct bond or -O-; p is 0, 1 or 2 and when p is 1 or 2 RA1 and RA2 are each independently hydrogen or (1-4C)alkyl; Z is carboxy or a mimic or bioisostere thereof.

Ouverture de dichlorocyclopropanes en presence d'un nucleophile interne. Absence de participation intramoleculaire. Rearrangement concerte en chlorures allyliques

It is shown that a conveniently placed internal nucleophile (carboxyl group) is not involved with the rearrangement of a diclorocyclopropane into an allylic chloride.This result appears to support a concerted mechanism of a ?s2 + ?a2 type for this rearrangement.In the products obtained, the allylic chloride may undergo displacement either by solvent (H2O), leading to alcohols, or by the internal carboxyl group, leading to a lactone.