Atomfair 1-(4-Chlorophenyl)propan-1-ol C9H11ClO

Description 1-(4-Chlorophenyl)propan-1-ol (CAS No. 13856-85-4) is a high-purity organic compound with the molecular formula C9H11ClO , widely utilized in pharmaceutical and chemical research. This aromatic alcohol features a chlorophenyl group attached to a propanol chain, making it a valuable intermediate in synthetic organic chemistry. Its IUPAC name, 1-(4-chlorophenyl)propan-1-ol , reflects its precise structural configuration. Available in various quantities, this compound is rigorously tested for purity and consistency, ensuring optimal performance in laboratory and industrial applications. Suitable for use in nucleophilic substitutions, esterifications, and as a chiral building block, it is an essential reagent for researchers and scientists.

Description

1-(4-Chlorophenyl)propan-1-ol (CAS No. 13856-85-4) is a high-purity organic compound with the molecular formula C₉H₁₁ClO, widely utilized in pharmaceutical and chemical research. This aromatic alcohol features a chlorophenyl group attached to a propanol chain, making it a valuable intermediate in synthetic organic chemistry. Its IUPAC name, 1-(4-chlorophenyl)propan-1-ol, reflects its precise structural configuration. Available in various quantities, this compound is rigorously tested for purity and consistency, ensuring optimal performance in laboratory and industrial applications. Suitable for use in nucleophilic substitutions, esterifications, and as a chiral building block, it is an essential reagent for researchers and scientists.

CAS No: 13856-85-4
Molecular Formula: C9H11ClO
Molecular Weight: 170.63
Exact Mass: 170.0498427
Monoisotopic Mass: 170.0498427
IUPAC Name: 1-(4-chlorophenyl)propan-1-ol
SMILES: CCC(C1=CC=C(C=C1)Cl)O
Synonyms: 1-(4-chlorophenyl)propan-1-ol, 13856-85-4, 4-Chloro-alpha-ethylbenzyl alcohol, 1-(4-chlorophenyl)-1-propanol, (S)-1-(4-CHLOROPHENYL)-1-PROPANOL

Application

1-(4-Chlorophenyl)propan-1-ol serves as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. It is commonly employed in the preparation of chiral compounds and as a precursor for biologically active molecules. Researchers utilize this compound in asymmetric synthesis and catalysis studies due to its reactive hydroxyl group and aromatic chlorophenyl moiety. Its stability and well-defined structure make it ideal for method development and scale-up processes in organic chemistry.

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