37480-41-4

Usage

Uses

Used in Pharmaceutical Industry:
Cyclohexanecarboxylic acid, 1-methyl-4-oxo-, methyl ester is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique chemical structure allows it to be a versatile building block for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical industry, Cyclohexanecarboxylic acid, 1-methyl-4-oxo-, methyl ester is utilized as an intermediate in the production of various agrochemicals, such as pesticides and herbicides. Its chemical properties make it suitable for the synthesis of compounds that can effectively control pests and weeds in agricultural settings.
As an Intermediate in Chemical Synthesis:
Cyclohexanecarboxylic acid, 1-methyl-4-oxo-, methyl ester is used as an intermediate in the manufacturing of other chemicals. Its reactivity and functional groups make it a valuable component in the synthesis of a wide range of chemical products, contributing to various industries.

Upstream product

• 37480-31-2 4-methoxy-1-methyl-cyclohex-3-enecarboxylic acid methyl ester 
• 1523-89-3 methyl 1-methyl-4-oxo-2-cyclohexene-1-carboxylate 
• 825-04-7 methyl 1-methylcyclohexanecarboxylate 
• 186581-53-3 diazomethane 
• 24463-41-0 1-methyl-4-oxo-cyclohexanecarboxylic acid 

Downstream Products

• 24463-41-0 1-methyl-4-oxo-cyclohexanecarboxylic acid 
• 87787-08-4 methyl 4,4-ethylenedioxy-1-methylcyclohexanecarboxylate 
• 37480-42-5 methyl 4-hydroxy-1-methylcyclohexanecarboxylate 
• 62618-04-6 4-Aminomethyl-1-methyl-cyclohexanecarboxylic acid 
• 62618-03-5 4-Aminomethyl-1-methyl-cyclohexanecarboxylic acid 
• 73845-88-2 t-1-Methyl-t-4,r-1-cyclohexandicarbonsaeure 
• 73845-86-0 1-Methyl-3-cyclohexen-1,4-dicarbonsaeure 
• 69082-04-8 4-(4-methoxy-phenyl)-1-methyl-cyclohexanecarboxylic acid 
• 87787-20-0 2-[4-Methyl-4-(4-nitro-phenoxymethyl)-cyclohexyloxy]-tetrahydro-pyran 
• 87787-39-1 5-<4-(c-4-hydroxy-1-methyl-r-1-cyclohexylmethoxy)benzyl>-2,4-thiazolidinedione 
• 93392-66-6 5-<4-(c-4-hydroxy-1-methyl-r-1-cyclohexylmethoxy)benzyl>-2-imino-4-thiazolidinone 
• 93392-65-5 methyl 2-bromo-3-<4-(c-4-hydroxy-1-methyl-r-1-cyclohexylmethoxy)phenyl>propionate 
• 87787-14-2 4-(c-4-hydroxy-1-methyl-r-1-cyclohexylmethoxy)nitrobenzene 
• 93392-64-4 methyl 1-methyl-c-4(2-tetrahydropyranyloxy)-r-1-cyclohexanecarboxylate 

Relevant academic research and scientific papers

N-Ammonium Ylide Mediators for Electrochemical C-H Oxidation

The site-specific oxidation of strong C(sp3)-H bonds is of uncontested utility in organic synthesis. From simplifying access to metabolites and late-stage diversification of lead compounds to truncating retrosynthetic plans, there is a growing need for new reagents and methods for achieving such a transformation in both academic and industrial circles. One main drawback of current chemical reagents is the lack of diversity with regard to structure and reactivity that prevents a combinatorial approach for rapid screening to be employed. In that regard, directed evolution still holds the greatest promise for achieving complex C-H oxidations in a variety of complex settings. Herein we present a rationally designed platform that provides a step toward this challenge using N-ammonium ylides as electrochemically driven oxidants for site-specific, chemoselective C(sp3)-H oxidation. By taking a first-principles approach guided by computation, these new mediators were identified and rapidly expanded into a library using ubiquitous building blocks and trivial synthesis techniques. The ylide-based approach to C-H oxidation exhibits tunable selectivity that is often exclusive to this class of oxidants and can be applied to real-world problems in the agricultural and pharmaceutical sectors.

Thiazolidine derivatives and production thereof

A thiazolidine derivative of the general formula, STR1 is a cyclohexane ring having an oxo or hydroxyl group as a substituent on any of the methylene groups constituting the ring and R is a hydrogen atom or a lower alkyl group having 1 to 4 carbon atoms,