Description

4-(4-Methylphenoxy)benzylamine hydrochloride (CAS No. 262862-66-8) is a high-purity organic compound with the molecular formula C₁₄H₁₆ClNO. This hydrochloride salt derivative of 4-(4-methylphenoxy)benzylamine is widely utilized in pharmaceutical and chemical research due to its stable crystalline form and well-defined structure. The IUPAC name, [4-(4-methylphenoxy)phenyl]methanamine;hydrochloride, reflects its precise chemical composition, featuring a benzylamine core substituted with a 4-methylphenoxy group. Ideal for synthetic applications, this compound is supplied with rigorous quality control to ensure consistency in reactivity and purity (≥95% by HPLC). Suitable for use in medicinal chemistry, it serves as a key intermediate in the development of bioactive molecules. Store in a cool, dry place under inert conditions to maintain stability.

Properties

• CAS Number: 262862-66-8
• Complexity: 191
• IUPAC Name: [4-(4-methylphenoxy)phenyl]methanamine;hydrochloride
• InChI: InChI=1S/C14H15NO.ClH/c1-11-2-6-13(7-3-11)16-14-8-4-12(10-15)5-9-14;/h2-9H,10,15H2,1H3;1H
• InChI Key: PYSIBOVVDDDETB-UHFFFAOYSA-N
• Exact Mass: 249.0920418
• Molecular Formula: C14H16ClNO
• Molecular Weight: 249.73
• SMILES: CC1=CC=C(C=C1)OC2=CC=C(C=C2)CN.Cl
• Topological: 35.3
• Monoisotopic Mass: 249.0920418
• Synonyms: 262862-66-8, 4-(4-Methylphenoxy)benzylamine hydrochloride, 4-(4-METHYLPHENOXY)BENZYLAMINE HCL, (4-(p-tolyloxy)phenyl)methanamine hydrochloride, 4-(4-Methylphenoxy)benzylamine, HCl, [4-(4-Methylphenoxy)Phenyl]Methanamine Hydrochloride, [4-(4-methylphenoxy)phenyl]methanamine;hydrochloride, [4-(4-Methylphenoxy)phenyl]methylamine hydrochloride, MFCD02089411, SCHEMBL6160193, DTXSID80590035, AR1874, AKOS022182187, AS-45227, 4-(4-Methylphenoxy)benzylaminehydrochloride, CS-0073025, SR-01000368630, SR-01000368630-1, F9994-0681, 1-[4-(4-METHYLPHENOXY)PHENYL]METHANAMINE HYDROCHLORIDE, 1-[4-(4-Methylphenoxy)phenyl]methanamine–hydrogen chloride (1/1)

Application

4-(4-Methylphenoxy)benzylamine hydrochloride is primarily employed as a versatile building block in organic synthesis, particularly in the preparation of pharmacologically active compounds. Researchers leverage its reactive amine group for coupling reactions or further functionalization in drug discovery. It has shown utility in the development of CNS-targeting agents due to its aromatic and phenoxy motifs. Additionally, this compound is explored in material science for designing advanced polymers with tailored properties.

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