Description

N-(2-Methyl-3-nitrophenethyl)-N-propylpropan-1-amine hydrochloride (CAS No. 920986-68-1) is a high-purity synthetic organic compound with the molecular formula C₁₅H₂₅ClN₂O₂. This hydrochloride salt is characterized by its fine crystalline structure and excellent solubility in polar organic solvents, making it suitable for a variety of research and pharmaceutical applications. It is synthesized under strict quality control to ensure >98% purity, as verified by HPLC and NMR analysis. The compound features a 2-methyl-3-nitrophenethyl backbone with dipropylamine substitution, offering unique reactivity for chemical modifications. Proper storage at 2-8°C in a tightly sealed container is recommended to maintain stability.

Properties

• CAS Number: 920986-68-1
• Complexity: 259
• IUPAC Name: N-[2-(2-methyl-3-nitro-phenyl)ethyl]-N-propyl-propan-1-amine;hydrochloride
• InChI: InChI=1S/C15H24N2O2.ClH/c1-4-10-16(11-5-2)12-9-14-7-6-8-15(13(14)3)17(18)19;/h6-8H,4-5,9-12H2,1-3H3;1H
• InChI Key: WGCKLIPNNADOCJ-UHFFFAOYSA-N
• Exact Mass: 300.1604557
• Molecular Formula: C15H25ClN2O2
• Molecular Weight: 300.82
• SMILES: CCCN(CCC)CCC1=C(C(=CC=C1)[N+](=O)[O-])C.Cl
• Topological: 49.1
• Monoisotopic Mass: 300.1604557
• Synonyms: 920986-68-1, N-(2-Methyl-3-nitrophenethyl)-N-propylpropan-1-amine hydrochloride, [2-(2-Methyl-3-nitro-phenyl)-ethyl]-dipropyl-amine hydrochloride, 2-(2-METHYL-3-NITRO-PHENYL)-ETHYL]-DIPROPYL-AMINE HCL, SCHEMBL2012002, DTXSID00659299, AKOS022172762, N-[2-(2-methyl-3-nitrophenyl)ethyl]-N-propylpropan-1-amine;hydrochloride, DB-127819, N-(2-Methyl-3-Nitrophenethyl) N-Propylpropane-1-Amine HCl, 2-Methyl-3-nitro-N,N-dipropylbenzeneethanamine hydrochloride, N-[2-(2-methyl-3-nitrophenyl)ethyl]-N-propylpropan-1-amine hydrochloride, N-[2-(2-Methyl-3-nitrophenyl)ethyl]-N-propylpropan-1-amine–hydrogen chloride (1/1)

This compound serves as a key intermediate in the synthesis of bioactive molecules, particularly in pharmaceutical research targeting CNS disorders. Its structural features make it valuable for studying neurotransmitter modulation and receptor interactions. Researchers utilize it in preclinical studies to investigate potential therapeutic effects. The nitrophenyl group enables further functionalization for probe development.

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