Description

trans-4′-Propyl-(1,1′-bicyclohexyl)-4-carboxylic Acid (CAS: 65355-32-0) is a high-purity, synthetic carboxylic acid derivative with the molecular formula C₁₆H₂₈O₂. This compound features a bicyclohexyl backbone substituted with a propyl group and a carboxylic acid functionality, offering unique steric and electronic properties. It is widely utilized in advanced organic synthesis, pharmaceutical research, and material science due to its rigid cyclohexyl rings and versatile reactivity. Available in ≥98% purity (HPLC), it is supplied as a white to off-white crystalline powder, ensuring consistent performance in sensitive applications. Ideal for use as an intermediate in liquid crystal displays (LCDs), chiral auxiliaries, and ligand design.

Properties

• CAS Number: 65355-32-0
• Complexity: 258
• IUPAC Name: 4-(4-propylcyclohexyl)cyclohexanecarboxylic acid
• InChI: InChI=1S/C16H28O2/c1-2-3-12-4-6-13(7-5-12)14-8-10-15(11-9-14)16(17)18/h12-15H,2-11H2,1H3,(H,17,18)
• InChI Key: JXPGQFKJNKWDKP-UHFFFAOYSA-N
• Exact Mass: 252.208930132
• Molecular Formula: C16H28O2
• Molecular Weight: 252.39
• SMILES: CCCC1CCC(CC1)C2CCC(CC2)C(=O)O
• Topological: 37.3
• Monoisotopic Mass: 252.208930132
• Synonyms: 65355-32-0, trans-4′-Propyl-(1,1′-bicyclohexyl)-4-carboxylic Acid, 83860-51-9, 4-(4-propylcyclohexyl)cyclohexane-1-carboxylic Acid, [1,1′-Bicyclohexyl]-4-carboxylic acid, 4′-propyl-, (trans,trans)-, 4-(4-propylcyclohexyl)cyclohexanecarboxylic acid, 4′-Propyl-[1,1′-bicyclohexyl]-4-carboxylic acid, 4′-Propyl-[1,1′-bi(cyclohexane)]-4-carboxylic acid, 4′-propyl-1,1′-bi(cyclohexyl)-4-carboxylic acid, 4-(Trans-4-Propylcyclohexyl)cyclohexanecarboxylic acid, [1,1′-bicyclohexyl]-4-carboxylic acid, 4′-propyl-, 765943-71-3, (trans,trans)-4′-Propyl-[1,1′-bicyclohexyl]-4-carboxylic Acid; trans-4-(4-Propylcyclohexyl)cyclohexanecarboxylic Acid; trans-4-(trans-4-Propylcyclohexyl)cyclohexanecarboxylic Acid;, (Trans,Trans)-4-Propyl-[1,1-Bicyclohexyl]-4-Carboxylic Acid, 4′-Propylbi(cyclohexane)-4-carboxylic acid, Oprea1_318804, SCHEMBL1310398, SCHEMBL3275198, SCHEMBL4159283, SCHEMBL4159289, DTXSID401173830, DTXSID501184006, SBB059475, STK058310, AKOS005387317, AKOS015915060, AKOS024389708, CS-W010198, SB66329, 4′-propylbicyclohexane-4-carboxylic acid, 4-propyl-4′-bicyclohexanecarboxylic acid, 171337-48-7, DS-15537, LS-14541, DB-219032, ST51044454, N10454, 4′-Propyl-[1,1′-bicyclohexyl]-4-carboxylicacid, trans,trans-4′-n-Propylbicyclohexyl-4-carboxylic acid, trans-4-(trans-4′-propylcyclohexyl)cyclohexanecarboxylic acid, trans-4-(trans-4′-propyl cyclohexyl)-cyclohexane carboxylic acid, (trans,trans)-4a(2)-Propyl[1,1a(2)-bicyclohexyl]-4-carboxylic acid, [1,1a(2)-Bicyclohexyl]-4-carboxylic acid, 4a(2)-propyl-, (cis,trans)-

This compound serves as a key intermediate in the synthesis of liquid crystal materials for high-performance displays due to its stable trans-configuration and mesogenic properties. Researchers employ it in medicinal chemistry for scaffold modification and chiral resolution studies. Its rigid structure also makes it valuable in polymer science for enhancing thermal stability and mechanical properties. Additionally, it is explored in catalysis as a ligand precursor for transition metal complexes.

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