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Atomfair [1,1′-Bi(cyclohexane)]-4,4′-dicarbonyl dichloride C14H20Cl2O2
Description [1,1′-Bi(cyclohexane)]-4,4′-dicarbonyl dichloride (CAS: 25675-41-6) is a high-purity, bifunctional organic compound with the molecular formula C14H20Cl2O2. This crystalline solid is a valuable building block in synthetic organic chemistry, particularly for the preparation of polymers, dendrimers, and other advanced materials. Its IUPAC name, 4-(4-carbonochloridoylcyclohexyl)cyclohexane-1-carbonyl chloride , reflects its symmetrical structure featuring two reactive acyl chloride groups. With a molecular weight of 291.21 g/mol, this compound is soluble in common organic solvents like dichloromethane and THF. It is supplied with comprehensive analytical data including1H NMR,13C NMR, and HPLC purity reports. Store in a cool, dry place under inert atmosphere to maintain stability.
Description
Description
[1,1′-Bi(cyclohexane)]-4,4′-dicarbonyl dichloride (CAS: 25675-41-6) is a high-purity, bifunctional organic compound with the molecular formula C14H20Cl2O2. This crystalline solid is a valuable building block in synthetic organic chemistry, particularly for the preparation of polymers, dendrimers, and other advanced materials. Its IUPAC name, 4-(4-carbonochloridoylcyclohexyl)cyclohexane-1-carbonyl chloride, reflects its symmetrical structure featuring two reactive acyl chloride groups. With a molecular weight of 291.21 g/mol, this compound is soluble in common organic solvents like dichloromethane and THF. It is supplied with comprehensive analytical data including 1H NMR, 13C NMR, and HPLC purity reports. Store in a cool, dry place under inert atmosphere to maintain stability.
- CAS No: 25675-41-6
- Molecular Formula: C14H20Cl2O2
- Molecular Weight: 291.2
- Exact Mass: 290.0840353
- Monoisotopic Mass: 290.0840353
- IUPAC Name: 4-(4-carbonochloridoylcyclohexyl)cyclohexane-1-carbonyl chloride
- SMILES: C1CC(CCC1C2CCC(CC2)C(=O)Cl)C(=O)Cl
- Synonyms: SCHEMBL2153805, 25675-41-6, [1,1′-Bi(cyclohexane)]-4,4′-dicarbonyl dichloride
Application
This bifunctional acyl chloride is widely used as a linker in polymer chemistry for creating high-performance polyamides and polyesters. Researchers utilize it to synthesize novel dendritic structures with precise architectural control. The compound serves as a key intermediate in pharmaceutical development for creating active ingredient conjugates. Its symmetrical structure makes it particularly valuable for creating crosslinked materials with uniform properties.
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