71458-12-3

Usage

Uses

Used in Organic Synthesis:
Trans-1-(bromomethyl)-4-propylcyclohexane is used as a synthetic intermediate for the creation of various complex organic molecules. Its bromomethyl group allows for further functionalization and reaction with other compounds, making it a versatile component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Research Laboratories:
In research settings, Trans-1-(bromomethyl)-4-propylcyclohexane is utilized as a model compound to study reaction mechanisms and to develop new synthetic methodologies. Its unique structure provides opportunities for exploring novel chemical reactions and understanding the properties of halogenated cycloalkanes.
Used in Pharmaceutical Industry:
Trans-1-(bromomethyl)-4-propylcyclohexane is used as a precursor in the development of pharmaceutical compounds. Its reactivity and structural features can be leveraged to create new drug candidates with potential therapeutic applications.
Used in Agrochemical Industry:
Trans-1-(bromomethyl)-4-propylcyclohexane may also find use in the agrochemical sector as a starting material for the synthesis of pesticides or other agrochemical products, where its specific reactivity could be harnessed to create effective and targeted agents for crop protection.
Used in Materials Science:
Due to its structural attributes, Trans-1-(bromomethyl)-4-propylcyclohexane could be employed in the development of new materials with specialized properties, such as polymers with unique mechanical or chemical characteristics.
It is crucial to handle Trans-1-(bromomethyl)-4-propylcyclohexane with care due to its potential health and environmental risks, ensuring proper management and safety measures are in place throughout its use in various applications.

InChI:InChI=1/C10H19Br/c1-2-3-9-4-6-10(8-11)7-5-9/h9-10H,2-8H2,1H3/t9-,10-

Upstream product

• 67589-88-2 trans-4-propylcyclohexanecarbonyl chloride 
• 38289-27-9 trans-4-propyl-cyclohexanecarboxylic acid 
• 71458-06-5 trans-4-propyl-1-(hydroxymethyl)cyclohexane 

Downstream Products

• 95149-47-6 trans-4-propyl-1-(cyanomethyl)cyclohexane 
• 98614-27-8 2-Bromo-4-(4-propyl-cyclohexyl)-1-(4-propyl-cyclohexylmethoxy)-benzene 
• 92262-23-2 2-Bromo-4-[2-(4-heptyl-cyclohexyl)-ethyl]-1-(4-propyl-cyclohexylmethoxy)-benzene 
• 1023967-90-9 C₁₀H₁₉BrMg 
• 87430-00-0 4-(4-Propyl-cyclohexylmethoxy)-phenol 
• 73899-61-3 trans-4-propylcyclohexyl acetyl chloride 
• 71458-18-9 trans-4-propylcyclohexylacetic acid 
• 84361-31-9 [2-(4-Propyl-cyclohexyl)-ethyl]-benzene 
• 89013-09-2 4-[2-(4-Propyl-cyclohexyl)-ethyl]-benzoyl chloride 
• 89013-05-8 4-[2-(4-Propyl-cyclohexyl)-ethyl]-benzamide 
• 87002-34-4 1-Phenyl-2-(4-propyl-cyclohexyl)-ethanone 
• 86849-44-7 4-(2-trans-4-propylcyclohexyl-ethyl)-benzonitrile 

Relevant academic research and scientific papers

Nematic compounds

Nematic compounds with a negative DC antisotropy, characterized by the formula I STR1 in which m=1 or 2, r is zero or 1 and m+r=1 or 2, and R1 and R2 are identical or different and are selected from alkyl and alkoxy groups each havin

The Synthesis and Liquid-Crystal Transition Temperatures of Some Fluoro-Substituted Benzonitriles

Various laterally fluoro-substituted benzonitriles have been prepared containing a trans-4-(n-alkyl)cyclohexane ring linked to the 4-position of the benzonitriles either through a methyleneoxy (-CH2O-) or an ethylene (-CH2CH2-) bridge.The bridging group links the benzonitrile and cyclohexane rings either directly or through an additional 1,4-bonded cyclohexane or benzene ring.The synthesis and liquid-crystal transition temperatures of these new compounds are described.In several cases the nematic-isotropic transition temperatures of F-substituted benzonitriles are found to be higher than those of the non-laterally substituted analogues.

The Properties of Liquid Crystal Materials Incorporating the -CH2O- Inter-ring Linkage

To establish more securely the influence of the -CH2O- inter-ring linkage upon the properties of mesogens of both high and low dielectric anisotropy, a range of ethers with the following general structure has been prepared and their properties examined. The thermal and electro-optic properties of the compounds are discussed, and comparisons made where possible with analogous materials incorporating the -CH2CH2- linkage.

SYNTHESIS AND SOME PHYSICAL PROPERTIES OF 1-CYCLOHEXYL-2-(4 double prime -HALOBIPHENYL-4 prime -yl)ETHANES.

A series of 1-(trans-4 prime -n-alkylcyclohexyl)-2-(4 double prime -halobiphenyl-4 prime -yl)ethanes, which show nematic phases, was prepared. Their transition temperatures, enthalpies and entropies were measured. Their bulk viscosities, birefringences and dielectric constants were determined by extrapolation. The bulk viscosity as a function of the third power of the van der Waals radius of the halogeno group, the birefringence as a function of the van der Waals radius of the halogeno group, and the dielectric constants as a function of the dipole moment of the halogeno group are discussed for the 1-(trans-4 prime -n-propylcyclohexyl)-2-(4 double prime -halobiphenyl-4 prime -yl)ethanes.

1-(TRANS-4 prime -N-ALKYLCYCLOHEXYL)-2-(4 double prime -CYANOPHENYL)ETHANES - A NEW SERIES OF STABLE NEMATOGENS OF POSITIVE DIELECTRIC ANISOTROPY.

The synthesis and some important properties of the 1-(trans-4 prime -n-alkylcyclohexyl)-2-(4 double prime -cyanophenyl)ethanes - where n-alkyl equals C//1 to C//7 - are described.