Description
4-(4-pentylcyclohexyl)benzoyl Chloride (CAS No. 73011-79-7) is a high-purity organic compound with the molecular formula C18H25ClO. This specialized reagent features a benzoyl chloride functional group attached to a 4-pentylcyclohexyl moiety, making it a valuable intermediate in synthetic organic chemistry and materials science. The compound is supplied as a clear to pale yellow liquid with a characteristic acyl chloride odor, and it should be handled under inert conditions due to its moisture sensitivity. With a molecular weight of 292.84 g/mol, this product is particularly useful for nucleophilic acyl substitution reactions, enabling the introduction of the 4-(4-pentylcyclohexyl)benzoyl group into target molecules. It is commonly employed in the synthesis of liquid crystals, pharmaceutical intermediates, and advanced organic materials. Our product is rigorously tested for purity and consistency, ensuring optimal performance in demanding research applications.
Properties
- CAS Number: 73011-79-7
- Complexity: 286
- IUPAC Name: 4-(4-pentylcyclohexyl)benzoyl chloride
- InChI: InChI=1S/C18H25ClO/c1-2-3-4-5-14-6-8-15(9-7-14)16-10-12-17(13-11-16)18(19)20/h10-15H,2-9H2,1H3
- InChI Key: LDCKYCPBTBCBQF-UHFFFAOYSA-N
- Exact Mass: 292.1593931
- Molecular Formula: C18H25ClO
- Molecular Weight: 292.8
- SMILES: CCCCCC1CCC(CC1)C2=CC=C(C=C2)C(=O)Cl
- Topological: 17.1
- Monoisotopic Mass: 292.1593931
- Synonyms: 73011-79-7, 4-(trans-4-Pentylcyclohexyl)benzoyl chloride, 4-(4-pentylcyclohexyl)benzoyl Chloride, 4-((1S,4R)-4-Pentylcyclohexyl)benzoyl chloride, 4-[(1s,4r)-4-pentylcyclohexyl]benzoyl chloride, SCHEMBL8556817, SCHEMBL9789185, LDCKYCPBTBCBQF-SHTZXODSSA-N, 4-(trans-4-Pentylcyclohexyl)benzoylchloride, F16557, p-(trans-4-pentylcyclohexyl)benzoic acid chloride, 4-(trans-4′-N-Pentylcyclohexyl)benzoic acid chloride
Application
4-(4-pentylcyclohexyl)benzoyl Chloride serves as a key synthetic intermediate in the production of liquid crystalline materials for display technologies. Researchers utilize this compound to prepare ester derivatives through reactions with phenolic compounds, which are then incorporated into nematic or smectic liquid crystal mixtures. The pentylcyclohexyl moiety contributes to the desired mesomorphic properties in these advanced materials. Additionally, this reagent finds application in medicinal chemistry for the synthesis of potential drug candidates with improved pharmacokinetic properties. Its reactivity as an acyl chloride makes it particularly valuable for creating amide or ester linkages in complex organic syntheses.
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