87787-02-8

Usage

Uses

Used in Pharmaceutical Industry:
Cyclohexanecarboxylic acid, 4-hydroxy-1-methyl-, methyl ester, transis used as a key intermediate in the synthesis of various pharmaceuticals. Its role in drug production is attributed to its unique chemical structure and reactivity, which allows for the creation of a wide range of medicinal compounds.
Used in Organic Synthesis:
Cyclohexanecarboxylic acid, 4-hydroxy-1-methyl-, methyl ester, transserves as an important building block in organic synthesis, enabling the formation of complex organic molecules. Its versatility in chemical reactions makes it a valuable component in the synthesis of various organic compounds.
Used in Cosmetic Industry:
Due to its antioxidant properties, Cyclohexanecarboxylic acid, 4-hydroxy-1-methyl-, methyl ester, transmay find applications in the cosmetic industry, where it can be used to enhance the stability and shelf life of cosmetic products.
Used in Food Industry:
The potential applications of Cyclohexanecarboxylic acid, 4-hydroxy-1-methyl-, methyl ester, trans- in the food industry could be related to its antioxidant characteristics, which may help in preserving the quality and extending the shelf life of food products.
It is crucial to note that the use of Cyclohexanecarboxylic acid, 4-hydroxy-1-methyl-, methyl ester, transin any industry must adhere to strict safety and regulatory guidelines to minimize health risks associated with exposure to this chemical compound.

Upstream product

• 6493-80-7 methyl 1-methyl-3-cyclohexenecarboxylate 

Downstream Products

• 93392-64-4 1-Methyl-4-(tetrahydro-pyran-2-yloxy)-cyclohexanecarboxylic acid methyl ester 
• 87787-20-0 2-[4-Methyl-4-(4-nitro-phenoxymethyl)-cyclohexyloxy]-tetrahydro-pyran 
• 87787-45-9 5-<4-(t-4-hydroxy-1-methyl-r-1-cyclohexylmethoxy)benzyl>-2,4-thiazolidinedione 
• 93392-63-3 5-<4-(t-4-hydroxy-1-methyl-r-1-cyclohexylmethoxy)benzyl>-2-imino-4-thiazolidinone 
• 93392-62-2 methyl 2-bromo-3-<4-(t-4-hydroxy-1-methyl-r-1-cyclohexylmethoxy)phenyl>propionate 
• 93392-67-7 4-(t-4-hydroxy-1-methyl-r-1-cyclohexylmethoxy)nitrobenzene 
• 87787-24-4 4-(4-Amino-phenoxymethyl)-4-methyl-cyclohexanol 
• 87787-12-0 1-methyl-t-4-(2-tetrahydropyranyloxy)-r-1-cyclohexanemethanol 

Relevant academic research and scientific papers

Design and synthesis of seco-oxysterol analogs as potential inhibitors of 3-hydroxy-3-methylglutaryl-coenzyme A (HMG-CoA) reductase gene transcription

The synthesis and biological activity of a series of seco-oxysterol analogs designed to be inhibitors of transcription of the gene for 3- hydroxy-3-methylglutaryl-Coenzyme A reductase (HMGR) are described. The compound possessing the most significant acti