170811-08-2

Usage

Uses

Used in Coatings Industry:
1,4-Cyclohexanedimethanol, mono(4-methylbenzenesulfonate), transis used as a key component in the formulation of high-performance coatings. It enhances the durability and resistance of the coatings, making them suitable for various applications where resistance to heat and chemicals is required.
Used in Adhesives Industry:
In the adhesives industry, 1,4-Cyclohexanedimethanol, mono(4-methylbenzenesulfonate), transis utilized as a building block for creating strong and stable adhesives. Its trans configuration ensures the formation of robust polymer chains that contribute to the adhesive's bonding strength and longevity.
Used in Plasticizers Industry:
1,4-Cyclohexanedimethanol, mono(4-methylbenzenesulfonate), transis employed as a plasticizer to improve the flexibility and workability of plastics. Its incorporation into plastic materials results in enhanced performance characteristics, making the plastics more suitable for a wide range of applications.
Used in Synthesis of Polymers and Resins:
1,4-Cyclohexanedimethanol, mono(4-methylbenzenesulfonate), transserves as a vital building block in the synthesis of various polymers and resins. Its unique properties allow for the creation of materials with improved thermal stability, chemical resistance, and mechanical properties, which are essential for high-performance applications.

Upstream product

• 3236-48-4 trans-1,4-Cyclohexanedimethanol 
• 98-59-9 p-toluenesulfonyl chloride 
• 105-08-8 bis-1,4-(hydroxymethyl)cyclohexane 
• 10412-78-9 trans-1,4-cyclohexylenedimethylene diacetate 
• 94-60-0 dimethyl 1,4-cyclohexane dicarboxylate 

Downstream Products

• 1658500-48-1 tert-butyl (2,6-dichloro-3-(((trans-4-methylcyclohexyl)methyl)amino)pyridin-4-yl)carbamate 
• 1658500-49-2 2,6-dichloro-N³-((trans-4-methylcyclohexyl)methyl)pyridine-3,4-diamine 
• 1616434-24-2 4,6-dichloro-3-(((trans)-4-methylcyclohexyl)methyl)-3H-imidazo[4,5-c]pyridine 
• 1616434-25-3 2-bromo-4,6-dichloro-3-(((trans)-4-methylcyclohexyl)methyl)-3H-imidazo[4,5-c]pyridine 
• 1616434-26-4 4,6-dichloro-3-[(trans-4-methylcyclohexyl)methyl]-2-[(3R)-3-phenylmorpholin-4-yl]-3H-imidazo[4,5-c]pyridine 
• 1616434-27-5 6-chloro-4-(5-chloropyridin-3-yl)-3-[(trans-4-methylcyclohexyl)methyl]-2-[(3R)-3-phenylmorpholin-4-yl]-3H-imidazo[4,5-c]pyridine 
• 1616434-28-6 4-(5-chloropyridin-3-yl)-3-[(trans-4-methylcyclohexyl)methyl]-2-[(3R)-3-phenylmorpholin-4-yl]-3H-imidazo[4,5-c]pyridine-6-carbonitrile 
• 1658500-50-5 4-(5-chloropyridin-3-yl)-N'-hydroxy-3-[(trans-4-methylcyclohexyl)methyl]-2-[(3R)-3-phenylmorpholin-4-yl]-3H-imidazo[4,5-c]pyridine-6-carboximidamide 
• 1616428-74-0 5-{4-(5-chloropyridin-3-yl)-3-[(trans-4-methylcyclohexyl)methyl]-2-[(3R)-3-phenylmorpholin-4-yl]-3H-imidazo[4,5-c]pyridin-6-yl}-1,3,4-oxadiazol-2(3H)-one 
• 1616431-67-4 methyl 4-(5-chloropyridin-3-yl)-3-[(trans-4-methylcyclohexyl)methyl]-2-[(3R)-3-phenylmorpholin-4-yl]-3H-imidazo[4,5-c]pyridine-6-carboxylate 
• 1658500-51-6 4-(5-chloropyridin-3-yl)-3-[(trans-4-methylcyclohexyl)methyl]-2-[(3R)-3-phenylmorpholin-4-yl]-3H-imidazo[4,5-c]pyridine-6-carbohydrazide 
• 1616434-31-1 2-bromo-4-(5-chloropyridin-3-yl)-3-(((trans)-4-methylcyclohexyl)methyl)-3H-imidazo[4,5-c]pyridine-6-carbonitrile 
• 1616434-29-7 6-chloro-4-(5-chloropyridin-3-yl)-3-(((trans)-4-methylcyclohexyl)methyl)-3H-imidazo[4,5-c]pyridine 
• 1616434-30-0 4-(5-chloropyridin-3-yl)-3-(((trans)-4-methylcyclohexyl)methyl)-3H-imidazo[4,5-c]pyridine-6-carbonitrile 

Relevant academic research and scientific papers

Lipase-mediated route to diastereo-pure tranexamic acid

Diastereomerically pure tranexamic acid has been prepared via a diastereomeric separation of a trans-/cis-mixture of 1,4-cyclohexanedimethanol using lipase PS (Pseudomonas sp. Amano).

Substituted Imidazopyridines as HDM2 Inhibitors

The present invention provides substituted imidazopyridines as described herein or a pharmaceutically acceptable salt or solvate thereof. The representative compounds are useful as inhibitors of the HDM2 protein. Also disclosed are pharmaceutical compositions comprising the above compounds and potential methods of treating cancer using the same.

Photoinduced electron transfer of carbazole-acceptor dyads in solution and in a polymer solid

Photoinduced charge separation (CS) of carbazole-acceptor dyads (Cz-S-A) in solutions and in a polymer solid was examined by the measurement of fluorescence decay. For the discussion of CS from the viewpoint of thermal fluctuations in a solution and in a polymer solid, the separation distance between the Cz donor moiety and acceptor moiety was fixed with a rigid spacer. The photoinduced CS was observed for various solutions with different dielectric constants ranging from 3.06 to 37.5 at room temperature. The rate constant kCS increased with an increase in the free energy gap of -ΔGCS, indicating that CS is in the normal region of the Marcus theory. The temperature dependence of CS in a solution from 183 to 296 K was quantitatively explained by an electron transfer (ET) formula where solvent motions are treated as a classical mode and vibrational motions of the reactant are treated as a quantum mode. On the other hand, the photoinduced CS was also observed for a polymer solid with polar cyano groups over a wide temperature range from 100 to 400 K, although most motions are highly restricted compared with those in a solution. Above the glass transition temperature (T g), CS was explained by the same ET formula as that in a solution with dielectric constants measured at a high frequency. Below Tg, CS was independent of temperature, indicating that CS is caused by nuclear tunneling at low temperatures.