98730-93-9

Usage

Uses

Used in Food and Beverage Industry:
Methyl 2-cyclopropyl-2-hydroxyacetate is used as a flavoring agent for its pleasant aroma, enhancing the taste and smell of various food and drink products.
Used in Fragrance and Perfume Industry:
Methyl 2-cyclopropyl-2-hydroxyacetate is used as a component in the production of various fragrances and perfumes, contributing to their appealing scents.
Used in Industrial Applications:
Methyl 2-cyclopropyl-2-hydroxyacetate has a wide range of industrial applications, including the synthesis of other chemicals and compounds. It is synthetically produced and requires careful handling to avoid skin and eye irritation.

Upstream product

• 6395-79-5 methyl 2-cyclopropyl-2-oxoacetate 
• 67-56-1 methanol 
• 5617-84-5 (+/-)-2-hydroxy-2-cyclopropylacetic acid 
• 5648-87-3 2-cyclopropyl-2-hydroxyacetonitrile 
• 13885-13-7 2-cyclopropyl-2-oxoacetic acid 
• 186581-53-3 diazomethane 
• 113686-28-5 (S)-2-hydroxy-2-cyclopropyletanoic acid 
• 765-43-5 Cyclopropyl methyl ketone 

Downstream Products

• 113686-30-9 (S)-2-O(MTPA)-2-cyclopropylacetic acid methyl ester 

Relevant academic research and scientific papers

ON THE MECHANISM OF HYDROGEN TRANSFER BY NICOTINAMIDE COENZYMES AND SOME DEHYDROGENASES

The course of the oxidation of 2,2-dimethylcyclopropylmethanol and 2,2,3,3-tetramethylcyclopropylmethanol by horse liver alcohol dehydrogenase and NAD+ has been investigated.In neither case were ring opened products detected which, in agreement with previous observations, provides no evidence for the intermediacy of radicals in these reactions.The stability of several substituted cyclopropyl-alkyl radicals has been investigated by e.s.r. spectroscopy and the results are discussed with respect to cyclopropane-containing probes of the mechanism of oxidation of lactate dehydrogenase.

Stereodivergence in the Ireland-Claisen Rearrangement of α-Alkoxy Esters

A systematic investigation into the Ireland-Claisen rearrangement of α-alkoxy esters is reported. In all cases, the use of KN(SiMe3)2 in toluene gave rearrangement products corresponding to a Z-enolate intermediate with excellent diastereoselectivity, presumably because of chelation control. On the other hand, chelation-controlled enolate formation could be overcome for most substrates through the use of lithium diisopropylamide (LDA) in tetrahydrofuran (THF).

Anesthetic compounds and related methods of use

Provided herein are compounds according to formula (I): Provided herein is also a pharmaceutical composition comprising a compound according to formula (I) and a pharmaceutically acceptable carrier, and a method for providing anesthesia in a subject by administering such a pharmaceutical composition.

ANESTHETIC COMPOUNDS AND RELATED METHODS OF USE

Provided herein are compounds according to formula (I): Provided herein is also a pharmaceutical composition comprising a compound according to formula (I) and a pharmaceutically acceptable carrier, and a method for providing anesthesia in a subject by administering such a pharmaceutical composition.