4351-02-4

Basic information

• Product Name: 2,2,6-trimethyl-cyclohexanecarboxylic acid
• Synonyms: 2,2,6-trimethyl-cyclohexanecarboxylic acid
• CAS NO: 4351-02-4
• Molecular Weight: 170.252
• Mol File: 4351-02-4.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 2,2,6-trimethyl-cyclohexanecarboxylic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 2,2,6-trimethyl-cyclohexanecarboxylic acid(4351-02-4)
• EPA Substance Registry System: 2,2,6-trimethyl-cyclohexanecarboxylic acid(4351-02-4)

Safety Data

• Hazardous Substances Data: 4351-02-4(Hazardous Substances Data)

Upstream product

• 564-24-9 (+/-)-α-cyclogeranic acid 
• 4350-74-7 (1R,6S)-2,2,6-trimethylcyclohexyl carbaldehyde 
• 471-90-9 2,6,6-trimethyl-cyclohex-1-enecarboxylic acid 
• 459-80-3 geranic acid 
• 35836-89-6 2,6,6-trimethyl-2-cycloheptenone 
• 861315-80-2 2,3-dibromo-2,6,6-trimethyl-cycloheptanone 
• 7647-01-0 hydrogenchloride 
• 4351-02-4 (+/-)-2,2,6c-trimethyl-cyclohexane-r-carboxylic acid 
• 64-19-7 acetic acid 
• 24359-06-6 (+/-)-2,2,6t-trimethyl-cyclohexane-r-carboxylic acid amide 

Downstream Products

• 52567-46-1 (+/-)-2.2.6t-trimethyl-cyclohexane-carboxylic acid-(1r)-chloride 
• 39704-96-6 (+/-)-(trans)-2,2,6-trimethylcyclohexylamine 
• 4351-02-4 (+/-)-2,2,6t-trimethyl-cyclohexane-r-carboxylic acid 
• 22471-55-2 2,2,6-trimethylcyclohexanecarboxylic acid ethyl ester 
• 34026-01-2 (+/-)-cis-2,2,6-trimethyl-1-hydroxymethyl-cyclohexane 
• 52567-47-2 (+/-)-2.2.6t-trimethyl-cyclohexane-carboxylic acid-(1r)-methyl ester 
• 22471-55-2 (+/-)-2.2.6t-trimethyl-cyclohexane-carboxylic acid-(1r)-ethyl ester 
• 27863-38-3 1-bromo-2,2,6-trimethyl-cyclohexanecarboxylic acid 
• 25631-58-7 6β-((1Ξ)-2,2,6ξ-trimethyl-cyclohexane-r-carbonylamino)-penicillanic acid 
• 52567-47-2 (+/-)-2.2.6c-trimethyl-cyclohexane-carboxylic acid-(1r)-methyl ester 

Relevant articles and documents

Gold supported on a mesoporous CeO2 matrix as an efficient catalyst in the selective aerobic oxidation of aldehydes in the liquid phase

Gold supported on CeO2 catalyses the selective aerobic oxidation of aliphatic and aromatic aldehydes better than other reported catalysts such as Pt/C/Bi materials; the activity is due to the nanometric particle size of Au and CeO2. The Royal Society of Chemistry 2005.

OPSIN-BINDING LIGANDS, COMPOSITIONS AND METHODS OF USE

Compounds and compositions of said compounds along with methods of use of compounds are disclosed for treating ophthalmic conditions related to mislocalization of opsin proteins, the misfolding of mutant opsin proteins and the production of toxic visual cycle products that accumulate in the eye. Compounds and compositions useful in the these methods, either alone or in combination with other therapeutic agents, are also described.