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Usage

Uses

Used in Chemical Synthesis Industry:
Cyclohexyl-1,4-dicarboxylchloride is used as a precursor for the production of plasticizers and resin intermediates, contributing to the synthesis of various industrial-grade chemicals.
Used in Plastics Industry:
Cyclohexyl-1,4-dicarboxylchloride is used as a chemical intermediate in the production of plasticizers, which are additives that increase the flexibility and workability of plastics.
Used in Resin Production:
Cyclohexyl-1,4-dicarboxylchloride is used as a chemical intermediate in the synthesis of resins, which are essential components in the manufacturing of various products such as coatings, adhesives, and composite materials.
Safety Precautions:
As with many chemicals of its kind, it is advised to handle Cyclohexyl-1,4-dicarboxylchloride with caution as it can cause skin and eye irritation. Proper safety measures should be taken to minimize the risk of exposure and potential health hazards.

Upstream product

• 619-81-8 cyclohexane-1,4-dicarboxylic acid 
• 619-82-9 trans-hexahydroterephthalic acid 
• 14571-47-2 (1s,4s)-cyclohexane-1,4-dicarbonyl dichloride 
• 94-60-0 dimethyl 1,4-cyclohexane dicarboxylate 

Downstream Products

• 4322-09-2 1,4-dicarbonyl-cyclohexane 
• 94-60-0 dimethyl 1,4-cyclohexane dicarboxylate 
• 133406-74-3 3,4-Dichloro-1-[4-(3,4-dichloro-butyryl)-cyclohexyl]-butan-1-one 
• 133406-75-4 3,4-Dichloro-1-[4-(3,4-dichloro-3-methyl-butyryl)-cyclohexyl]-3-methyl-butan-1-one 
• 945362-35-6 trans-4-benzoylcyclohexane-carboxylic acid 
• 1089572-43-9 N₁,N₄-bis(pyridin-4-yl)cyclohexane-1,4-dicarboxamide 
• 1938-00-7 1,4-diphenyl cyclohexane-1,4-dicarboxylate 
• 14818-30-5 trans-1,4-Bis-<1-oxo-3-methyl-4-methoxycarbonyl-buten-(3)-yl>-cyclohexan 
• 7006-80-6 N,N'-Di(2-chlorobenzyl)cyclohexane-trans-1,4-bis(carboxamide) 
• 57113-55-0 trans-1,4-(4'-n-Butoxyphenyl)cyclohexandicarboxylat 
• 72245-80-8 bis(4-pentyloxyphenyl) trans-1,4-cyclohexanedicarboxylate 
• 72213-12-8 trans-1,4-(4'-n-Hexyloxyphenyl)cyclohexandicarboxylat 
• 26379-55-5 Cyclohexane-1,4-dicarboxylic acid bis-(4-methoxy-phenyl) ester 

Relevant academic research and scientific papers

Direction of the Dipole Moment in the Ester Group

The directions of the dipole moments in esters RCOOR' in which R and R' are alkyl or aryl groups have been deduced by analysis of experimental values of dipole moments of six compounds containing two polar groups, one or both of which are esters.New determinations of molecular dipole moments are reported for dimethyl trans-1,4-cyclohexanedicarboxylate and for trans-1,4-cyclohexanediol diacetate.The moment of the ester group is directed (in the positive sense) at an angle τE=123 +/- 3 deg from the R-CO axis in both aromatic and aliphatic esters, formates excepted.

An improved acid chloride preparation via phase transfer catalysis

Phase transfer catalysis has been found to be effective for the rapid conversion of carboxylic acids in high yield to the corresponding acid chlorides. The procedure is well suited for acids that exhibit low solubilities in normal organic solvents.

METHOD FOR PRODUCING ACID HALIDE SOLUTION, MIXED SOLUTION, AND METHOD FOR PRODUCING MONOESTER COMPOUND

The present disclosure provides a method for producing an acid halide solution that is useful as a production intermediate or the like that allows industrially advantageous production of a polymerizable liquid crystal compound. The method for producing an

Method for preparing 1, 4-diphenyl cyclohexanedicarboxylate

The invention belongs to the field of chemical synthesis and specifically relates to a method for preparing 1, 4-diphenyl cyclohexanedicarboxylate. The method comprises the following steps: performinga reaction in a solvent under the action of a catalyst

As a polymer skeleton [...][...] compound and method of manufacturing same

PROBLEM TO BE SOLVED: To provide a dinaphthothiophene compound useful as a refractive index improver for a plastic optical material, and a polymer comprising a dinaphthothiophene skeleton.SOLUTION: The dinaphthothiophene compound of the present invention

POLYMERIZABLE COMPOUND AND OPTICALLY ANISOTROPIC BODY

PROBLEM TO BE SOLVED: To provide a polymerizable compound which has high storage stability and can form a film-like polymer while being difficult to cause alignment defects, where the film-like polymer is less likely to be separated from a substrate even when irradiated with ultraviolet for a long time. SOLUTION: The invention provides a compound represented by general formula (I), and a polymer thereof. A composition comprising the compound is useful as a polymerizable liquid crystal composition. (For example, the compound is bis[4-(acryloyloxyethoxy-ethoxy-ethoxy)phenyl]1,4-cyclohexanedicarboxylate.) SELECTED DRAWING: None COPYRIGHT: (C)2018,JPOandINPIT

acyl triazole derivative and its manufacturing method

PROBLEM TO BE SOLVED: To provide a novel acyl triazole derivative that can be synthesized at low cost by a convenient method, has a comparable reactivity to an acid chloride with an amine compound and an alcohol compound, and can be safely handled, and a method of manufacturing the same; the acyl triazole derivative that is useful as a reactant applied to polymerization reaction to be continued; and a monomer comprising the same.SOLUTION: An acyl triazole derivative is shown by formula (1). In the formula, A denotes a substituted arylene group, a 1,3-phenylene group, a bisarylene group, a polycyclic arylene group, an alkylene group or an aralkylene group.

POLYMERIZABLE COMPOUND, POLYMERIZABLE COMPOSITION, AND FILM

PROBLEM TO BE SOLVED: To provide a novel polymerizable compound available as a low birefringent liquid crystal, and a film such as a low birefringent phase difference film and a reflective film with high selectivity on a reflection wavelength range. SOLUT

POLYMERIZABLE COMPOUND, POLYMER, POLYMERIZABLE COMPOSITION, FILM, AND HALF MIRROR FOR DISPLAYING PROJECTION IMAGE

The present invention provides a polymerizable compound denoted by Formula (I): in the formula, Z1 and Z2 represent an arylene group, and the like, m represents 1 or 2, n represents an integer of 0 or 1, and when m is 2, n is 0, Lsu

Novel bivalent securinine mimetics as topoisomerase I inhibitors

A series of novel bivalent securinine mimetics incorporating different linkers between C-15 and C-15′ were synthesized and their topoisomerase I (Topo I) inhibitory activities evaluated. It was thus revealed that mimetic R2 incorporating a rigid m-substituted benzene linker exhibits Topo I inhibitory activity three times that of parent securinine. Comprehensive structure-activity relationship analyses in combination with docking studies were used to rationalize the potent activity of these bivalent mimetics. Mechanistic studies served to confirm the deductions arising from docking studies that the active bivalent mimetics not only inhibited complexation between Topo I and DNA but also stabilized the Topo I-DNA complex itself.