Description

Benzenamine, 2-[(4-chlorophenyl)thio]- (CAS No. 37750-29-1) is a high-purity organic compound with the molecular formula C₁₂H₁₀ClNS. This specialized chemical features a unique structural combination of an aniline moiety linked to a 4-chlorophenylthio group, making it a valuable intermediate in pharmaceutical and agrochemical research. With a molecular weight of 235.73 g/mol, this compound exhibits excellent stability under standard laboratory conditions and is supplied with comprehensive analytical data (including HPLC, GC-MS, and NMR) to ensure reproducibility. Its versatility as a building block enables applications in heterocyclic synthesis, ligand design, and material science. Packaged in amber glass vials under inert atmosphere to prevent degradation, this product is ideal for researchers requiring precise control over synthetic pathways.

Properties

• CAS Number: 37750-29-1
• Complexity: 192
• IUPAC Name: 2-(4-chlorophenyl)sulfanylaniline
• InChI: InChI=1S/C12H10ClNS/c13-9-5-7-10(8-6-9)15-12-4-2-1-3-11(12)14/h1-8H,14H2
• InChI Key: JZLUOCTZACJYNR-UHFFFAOYSA-N
• Exact Mass: 235.0222482
• Molecular Formula: C12H10ClNS
• Molecular Weight: 235.73
• SMILES: C1=CC=C(C(=C1)N)SC2=CC=C(C=C2)Cl
• Topological: 51.3
• Monoisotopic Mass: 235.0222482
• Synonyms: Benzenamine, 2-[(4-chlorophenyl)thio]-, Benzenamine, 2-((4-chlorophenyl)thio)-, 609-474-9, 37750-29-1, 2-[(4-chlorophenyl)thio]aniline, 2-Amino-4′-chlorodiphenyl sulfide, 2-((4-Chlorophenyl)thio)aniline, 2-[(4-chlorophenyl)sulfanyl]aniline, 2-(4-chlorophenyl)sulfanylaniline, 2-(4-Chlorophenylthio)aniline, NSC624237, 2-AMINO-4′-CHLORODIPHENYLSULFIDE, MFCD00467319, 2NH2Ph-S-4ClPh, EC 609-474-9, CHEMBL171433, SCHEMBL1713296, DTXSID30326962, ALBB-005931, 2-Aminophenyl 4-chlorophenyl sulfide, STK503630, AKOS000120209, SB80596, FC117101, NCI60_007290, DB-049188, CS-0269693, NS00004892, 2-((4-Chlorophenyl)thio)aniline hydrochloride, EN300-33994, F83431

This compound serves as a key precursor in the synthesis of bioactive molecules, particularly in the development of antimicrobial and antiviral agents. Researchers utilize its reactive amino and thioether groups for constructing complex heterocycles in medicinal chemistry projects. It also finds use in material science as a monomer for conductive polymers and in catalysis as a ligand scaffold. The chlorophenyl moiety enhances lipophilicity, making derivatives of this compound useful in pharmacokinetic studies.

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