13170-66-6

Basic information

• Product Name: Cyclohexyl-1,4-dicarboxylchloride
• Synonyms: Cyclohexyl-1,4-dicarboxylchloride;1,4-Cyclohexanedicarbonyl dichloride (9CI);Hexahydroterephthaloyl chloride;CYCLOHEXY 1,4 DICARBOXYLIQUE CHLORIDE;Cyclohexane-1,4-dicarbonyl dichloride;1,4-CYCLOHEXANEDICARBONYL DICHLORIDE
• CAS NO: 13170-66-6
• Molecular Formula: C₈H₁₀Cl₂O₂
• Molecular Weight: 209.071
• Product Categories: ACIDHALIDE
• Mol File: 13170-66-6.mol
• Article Data: 26

Chemical Properties

• Boiling Point: 97-97.5 °C(Press: 0.5 Torr)
• Appearance: /
• Density: 1.2845 g/cm3
• CAS DataBase Reference: Cyclohexyl-1,4-dicarboxylchloride(CAS DataBase Reference)
• NIST Chemistry Reference: Cyclohexyl-1,4-dicarboxylchloride(13170-66-6)
• EPA Substance Registry System: Cyclohexyl-1,4-dicarboxylchloride(13170-66-6)

Safety Data

• Hazardous Substances Data: 13170-66-6(Hazardous Substances Data)

Usage

Description

Cyclohexyl-1,4-dicarboxylchloride, also known as 1,4-Cyclohexanedicarbonyl chloride, is a widely used chemical compound that is a heavy colorless liquid with a strong, pungent odor. It is produced through several chemical processes involving cyclohexanone and is often used as a precursor to plasticizers and resin intermediates, operating within the larger framework of industrial-grade chemical synthesis.

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 
• 94-60-0 dimethyl 1,4-cyclohexane dicarboxylate 
• 14571-47-2 (1s,4s)-cyclohexane-1,4-dicarbonyl dichloride 

Downstream Products

• 4322-09-2 1,4-dicarbonyl-cyclohexane 
• 1254714-43-6 C₂₆H₃₀N₂O₆ 
• 1254714-41-4 C₂₈H₃₄N₂O₆ 
• 1938-00-7 1,4-diphenyl cyclohexane-1,4-dicarboxylate 
• 16813-46-0 N,N'-Bis-(2-chloroethyl)-trans-1,4-cyclohexandicarboxamid 
• 72213-11-7 trans-1,4-(4'-n-Propoxyphenyl)cyclohexandicarboxylat 
• 72213-13-9 trans-1,4-(4'-n-Heptyloxyphenyl)cyclohexandicarboxylat 
• 72213-09-3 di-(4'-n-octyloxyphenyl)-trans-cyclohexane-1,4'-dicarboxylate 
• 72213-14-0 trans-1,4-(4'-n-Decyloxyphenyl)cyclohexandicarboxylat 
• 72213-15-1 trans-1,4-(4'-n-Dodecyloxyphenyl)cyclohexandicarboxylat 
• 72213-10-6 trans-1,4-(4'-n-Ethoxyphenyl)cyclohexandicarboxylat 

Relevant articles and documents

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.

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

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

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.