38792-89-1

Usage

Uses

Used in the Paint and Coating Industry:
N-PENTYLCYCLOHEXANE is used as a solvent to facilitate the application and drying process of paints, varnishes, and other coatings. Its low reactivity and stability contribute to the production of high-quality and durable coatings.
Used in the Adhesive Industry:
In the manufacturing of adhesives, N-PENTYLCYCLOHEXANE serves as a solvent that helps in the proper mixing and application of adhesive components, ensuring strong bonding and adherence properties.
Used in Pharmaceutical Production:
N-PENTYLCYCLOHEXANE is utilized in the production of pharmaceuticals, where it acts as a solvent or a synthetic intermediate, aiding in the synthesis of various medicinal compounds.
Used in Organic Chemistry:
As a synthetic intermediate in organic chemistry, N-PENTYLCYCLOHEXANE plays a crucial role in the synthesis of complex organic molecules, contributing to the development of new chemical entities and materials.

Upstream product

• 26311-45-5 4-pentylbenzoic acid 

Downstream Products

• 136101-38-7 4-Pentyl-cyclohexanecarboxylic acid 4-(2,2,2-trifluoro-acetyl)-phenyl ester 
• 128140-38-5 4-Pentyl-cyclohexanecarboxylic acid 4-(2,2,2-trifluoro-ethoxy)-phenyl ester 
• 67679-85-0 trans-4-pentylcyclohexane carboxylic acid chloride 
• 83811-40-9 4-formylphenyl 4-pentyl-cyclohexanecarboxylate 
• 170573-30-5 trans-(4-pentylcyclohexane)-methanol 
• 88074-85-5 trans-4-pentylcyclohexanecarboxylic acid p-ethynylphenyl ester 
• 402955-97-9 4-(4-pentynyloxy)phenyl trans-4-n-pentylcyclohexanoate 
• 402956-00-7 4-pentyl-cyclohexanecarboxylic acid 4-hex-5-ynyloxy-phenyl ester 

Relevant academic research and scientific papers

Improved synthesis of trans-4-alkylcyclohexane carboxylic acids

Several stereomerically pure amino acid derivatives containing the N-terminal trans-4-alkylcyclohexanoyl fragment were obtained. Hydrogenation of 4-alkylbenzoic acids in the presence of a special Ru-Ni/C catalytic system and isomerization of the resulting mixture of trans- and cis-isomers of 4-alkylcyclohexanecarboxylic acids were used as the key steps. The stereomeric configuration of all compounds was confirmed by 1H NMR spectroscopy. The compounds obtained possess a broad biological activity potential and are useful intermediates in the synthesis of stereomerically pure modified peptides.

Long-acting androgenic compounds and pharmaceutical compositions thereof

Long-acting androgenic compositions comprising C 4 -C 6 cycloalkyl carboxylic acids of testosterone and a pharmaceutically acceptable carrier medium. The ester can be dissolved in an acceptable oily medium or suspended in an aqueous medium in the form of

Synthesis and Liquid Crystalline Phases of Pyridazine Derivatives II

Four more pyridazine compounds were synthesized.The compounds have a general structure R-X-Y-Z-R'; where Y is 3,6 disubstituted pyridazine ring, X and Z are either trans cyclohexyl or phenyl rings, R and R' are n-alkyl groups.The structure assignments were confirmed by carbon 13 NMR.Their liquid crystalline properties were evaluated.When both X and Z are cyclohexyl rings, the compounds have a single smectic b phase.However, if a phenyl ring is introduced into the system, the morphology becomes complicated.Keywords: synthesis, pyridazine, smectic, classification