Description

1-Naphthylamine, 1,2,3,4-tetrahydro-, hydrochloride (CAS No. 49800-23-9) is a high-purity organic compound with the molecular formula C₁₀H₁₄ClN. This hydrochloride salt derivative of 1,2,3,4-tetrahydronaphthalen-1-amine is widely utilized in pharmaceutical research, chemical synthesis, and material science due to its stable crystalline form and high reactivity. With a purity of ≥98%, this product is ideal for laboratory use, offering consistent performance in nucleophilic substitution reactions, catalyst development, and as a precursor for heterocyclic compounds. Packaged under inert conditions to ensure stability, it is supplied in various quantities to meet both small-scale research and bulk industrial demands.

Properties

• CAS Number: 49800-23-9
• Complexity: 133
• IUPAC Name: tetralin-1-amine;hydrochloride
• InChI: InChI=1S/C10H13N.ClH/c11-10-7-3-5-8-4-1-2-6-9(8)10;/h1-2,4,6,10H,3,5,7,11H2;1H
• InChI Key: DETWFIUAXSWCIK-UHFFFAOYSA-N
• Exact Mass: 183.0814771
• Molecular Formula: C10H14ClN
• Molecular Weight: 183.68
• SMILES: C1CC(C2=CC=CC=C2C1)N.Cl
• Topological: 26
• Monoisotopic Mass: 183.0814771
• Synonyms: 1,2,3,4-Tetrahydro-1-naphthylamine hydrochloride, 1-NAPHTHYLAMINE, 1,2,3,4-TETRAHYDRO-, HYDROCHLORIDE, EINECS 222-397-1, 621-523-6, 1,2,3,4-Tetrahydronaphthalen-1-amine hydrochloride, 49800-23-9, 3459-02-7, 1,2,3,4-tetrahydronaphthalen-1-amine;hydrochloride, 1,2,3,4-TETRAHYDRO-1-NAPHTHYLAMINE HCL, aminotetralin hydrochloride, SCHEMBL2481580, DTXSID60956094, MFCD00051984, SBB000241, (1S)-Tetralin-1-amine hydrochloride, AKOS015903485, AC-5740, DS-16227, FT170170, 1,2,3,4-tetrahydronaphthylamine, chloride, DB-025132, DB-190697, CS-0131597, ST50407304, F16883, 1,2,3,4-Tetrahydronaphthalen-1-aminehydrochloride, 1,2,3,4-Tetrahydro-1-naphthylamine hydrochloride, 98%, Z316170348, 1,2,3,4-Tetrahydro-1-naphthalenamine hydrochloride (1:1)

This compound serves as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system (CNS) agents and bioactive molecules. It is also employed in organic synthesis for constructing tetralin-based frameworks and as a chiral building block for asymmetric catalysis. Researchers value its utility in studying neurotransmitter analogs and receptor-binding assays.

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