943-29-3

Basic information

• Product Name: trans-4-tert-Butylcyclohexanecarboxylic acid
• Synonyms: TRANS-4-TERT-BUTYLCYCLOHEXANECARBOXYLIC ACID;4-TERT-BUTYCYCLOHEXANECARBOXYLIC ACID;Cyclohexanecarboxylic acid, 4-tert-butyl-, trans-;4-TERT-BUTYLCYCLOHEXANECARBOXYLIC ACID (TRANS);(1α,4β)-4-tert-Butylcyclohexanecarboxylic acid;(1β)-4α-tert-Butylcyclohexanecarboxylic acid;trans-4-tert-Butylcyclohexanecarboxylic acid,97%;trans-4-tert-Butylcy
• CAS NO: 943-29-3
• Molecular Formula: C₁₁H₂₀O₂
• Molecular Weight: 184.28
• Product Categories: Biphenyl & Diphenyl ether;4-Substituted Cyclohexanecarboxylic Acids
• Mol File: 943-29-3.mol
• Article Data: 13

Chemical Properties

• Melting Point: 170-175 °C
• Boiling Point: 282.9 °C at 760 mmHg
• Flash Point: 136.7 °C
• Appearance: white fine crystalline powder
• Density: 0.996 g/cm³
• Vapor Pressure: 0.000852mmHg at 25°C
• Refractive Index: 1.473
• Storage Temp.: Sealed in dry,Room Temperature
• PKA: 4.92±0.10(Predicted)
• CAS DataBase Reference: trans-4-tert-Butylcyclohexanecarboxylic acid(CAS DataBase Reference)
• NIST Chemistry Reference: trans-4-tert-Butylcyclohexanecarboxylic acid(943-29-3)
• EPA Substance Registry System: trans-4-tert-Butylcyclohexanecarboxylic acid(943-29-3)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 37/39-26
• Hazardous Substances Data: 943-29-3(Hazardous Substances Data)

Usage

Chemical Properties

white fine crystalline powder

InChI:InChI=1/C11H20O2/c1-11(2,3)9-6-4-8(5-7-9)10(12)13/h8-9H,4-7H2,1-3H3,(H,12,13)/t8-,9-

Upstream product

• 98-73-7 4-(1,1-dimethylethyl)benzoic acid 
• 124-38-9 carbon dioxide 
• 5009-36-9 cis-1-bromo-4-tert-butylcyclohexane 
• 201230-82-2 carbon monoxide 
• 3178-22-1 tert-butylcyclohexane 
• 943-28-2 cis-4-t-butylcyclohexanecarboxylic acid 
• 19091-08-8 methyl 4-tert-butyl-cyclohexanecarboxylate 
• 114297-17-5 methyl trans-3-tert-butylcyclohexanecarboxylate 
• 98-52-2 4-(1,1-dimethylethyl)-cyclohexanol 
• 943-27-1 4'-t-butylacetophenone 
• 5451-55-8 4-tert-butylcyclohexanecarboxylic acid 

Downstream Products

• 5009-37-0 trans-1-bromo-4-tert-butylcyclohexane 
• 5009-36-9 cis-1-bromo-4-tert-butylcyclohexane 
• 2163-34-0 trans-4-t-butylcyclohexylamine 
• 17177-75-2 methyl ester of trans-4-tert-butylcyclohexanecarboxylic acid 
• 22523-17-7 4-tert-Butyl-cyclohexanecarboxylic acid 2-dimethylamino-ethyl ester 
• 15619-10-0 trans-1-(4'-t-butylcyclohexyl)-1-ethanone 
• 907-04-0 bis-(trans-4-tert-butyl-cyclohexanecarbonyl)-peroxide 
• 10601-39-5 trans-(4-tert-butyl-cyclohexyl)-methanol 
• 28467-42-7 trans-4-t-butylcyclohexanecarbonyl chloride 
• 10601-40-8 Toluolsulfonsaeure-(4)- 
• 29708-15-4 acide t.butyl-4 cyclohexane peroxycarboxylique trans 
• 27069-57-4 1-Methyl-trans-4-tert-butylcyclohexanecarboxylic acid 
• 31752-57-5 1-Methyl-cis-4-tert-butylcyclohexanecarboxylic acid 
• 15619-12-2 trans-4-tert.-Butyl-<2-hydroxypropyl-(2)>-cyclohexan 

Relevant articles and documents

Electrocatalytic hydrogenation of benzoic acids in a proton-exchange membrane reactor

The highly efficient chemoselective electrocatalytic hydrogenation of benzoic acids (BAs) to cyclohexanecarboxylic acids (CCAs) was carried out in a proton-exchange membrane reactor under mild conditions without hydrogenation of the carboxyl group. Among the investigated catalysts, the PtRu alloy catalyst was found to be the most suitable for achieving high current efficiencies for production of CCAs. An electrochemical spillover mechanism on the PtRu alloy catalyst was also proposed.

5-ETHYL-IMIDAZO (5,1-F) (1,2,4,) TRIAZIN-4 (3H) -ONES AS PHOSPHODIESTERASE INHIBITORS

The invention relates to novel 5-ethyl-imidazotriazinones, processes for their preparation and their use in medicaments, esp. for the treatment and/or prophylaxis of inflammatory processes and/or immune diseases.

Pd-Catalyzed Regio- and Stereo-selective Carboxylation of Cycloalkanes with CO

The reactions of cycloalkanes with CO via the C-H bond activation by Pd(OAc)2 catalyst have been found to proceed regio- and stereo-selectively to give corresponding carboxylic acids.The reactivity of C-H bonds of cycloalkanes decreases in the order: tert- > sec- > prim-carbon, and the stereochemistry of the substitutents on the main products is all equatorial.