1-(4-Chlorophenyl)-1-phenylethanol
Product Specifications
- CAS
- 59767-24-7
- Molecular Formula
- C14H13ClO
- Appearance
- yellow or brown liquid
- Synonym(s)
- 1-(p-Chlorophenyl)-1-phenylethanol; 4-Chloro-α-methyl-α-phenylbenzenemethanol; α-Methyl-α-phenyl-4-chlorobenzenemethanol; CleMastineFuMarateIMpurityC; ClemastineImpurity3(EPImpurityC); ClemastineEPImpurityC; ClemastineFumarateEPImpurityC
- Shipping
- ambient temperature
- Storage
- 2-8°C
- SMILES
- CC(C1=CC=CC=C1)(C2=CC=C(C=C2)Cl)O
- InChI
- InChI=1S/C14H13ClO/c1-14(16,11-5-3-2-4-6-11)12-7-9-13(15)10-8-12/h2-10,16H,1H3
Product Information
1-(4-Chlorophenyl)-1-phenylethanol has CAS 59767-24-7 and molecular formula C14H13ClO. PubChem links this CAS to one compound, CID 14189996, and gives molecular weight 232.70. The verified connectivity is SMILES CC(C1=CC=CC=C1)(C2=CC=C(C=C2)Cl)O, while InChIKey MHJLXHJZQCHSIT-UHFFFAOYSA-N supplies a compact identifier for the same neutral graph.
The alcohol carbon is bonded to a methyl group, an unsubstituted phenyl ring, and a second phenyl ring bearing chlorine para to the attachment. Together with the hydroxy group, these four different substituents make that carbon a stereogenic center. However, the PubChem record and SMILES used here do not specify its configuration, so this identity represents unspecified stereochemistry rather than a named enantiomer. Retaining the `4-chlorophenyl` locant separates the structure from ortho- or meta-chlorinated analogues with the same formula.
To make a structure-specific inquiry to Rlavie, state CAS 59767-24-7, the exact product name, and the requested quantity. Include a MOL or SDF structure file and indicate whether the intended graph has unspecified or explicitly defined stereochemistry. It can then be reconciled with PubChem CID 14189996, SMILES CC(C1=CC=CC=C1)(C2=CC=C(C=C2)Cl)O, and InChIKey MHJLXHJZQCHSIT-UHFFFAOYSA-N before request-specific details are addressed. The formula alone neither fixes the para chlorine position nor communicates any stereochemical expectation at the tertiary alcohol carbon. That distinction remains essential.