Atomfair 1-Benzyl-1,2,3,4-tetrahydroisoquinoline 1BnTIQ C16H17N CAS 19716-56-4

1-Benzyl-1,2,3,4-tetrahydroisoquinoline (CAS No. 19716-56-4) is a high-purity organic compound with the molecular formula C16H17N . This heterocyclic amine features a tetrahydroisoquinoline core substituted with a benzyl group at the 1-position, making it a valuable intermediate in pharmaceutical and chemical synthesis. Its well-defined structure and reactivity enable applications in medicinal chemistry, particularly in the development of bioactive molecules. Available in various quantities, this compound is rigorously tested for quality, ensuring optimal performance in research and industrial applications. Store in a cool, dry place under inert conditions to maintain stability.

Description

1-Benzyl-1,2,3,4-tetrahydroisoquinoline (CAS No. 19716-56-4) is a high-purity organic compound with the molecular formula C16H17N. This heterocyclic amine features a tetrahydroisoquinoline core substituted with a benzyl group at the 1-position, making it a valuable intermediate in pharmaceutical and chemical synthesis. Its well-defined structure and reactivity enable applications in medicinal chemistry, particularly in the development of bioactive molecules. Available in various quantities, this compound is rigorously tested for quality, ensuring optimal performance in research and industrial applications. Store in a cool, dry place under inert conditions to maintain stability.

Properties

  • CAS Number: 19716-56-4
  • Complexity: 232
  • IUPAC Name: 1-benzyl-1,2,3,4-tetrahydroisoquinoline
  • InChI: InChI=1S/C16H17N/c1-2-6-13(7-3-1)12-16-15-9-5-4-8-14(15)10-11-17-16/h1-9,16-17H,10-12H2
  • InChI Key: YRYCIFUZSUMAAY-UHFFFAOYSA-N
  • Exact Mass: 223.136099547
  • Molecular Formula: C16H17N
  • Molecular Weight: 223.31
  • SMILES: C1CNC(C2=CC=CC=C21)CC3=CC=CC=C3
  • Topological: 12
  • Monoisotopic Mass: 223.136099547
  • Physical Description: Solid
  • Synonyms: 1-Benzyl-1,2,3,4-tetrahydroisoquinoline, 19716-56-4, 1BnTIQ, 1-benzyl-1,2,3,4-tetrahydro-isoquinoline, 1,2,3,4-Tetrahydro-1-(phenylmethyl)isoquinoline, (R,S)-Tetrahydrobenzylisoquinoline, (RS)-1-Benzyl-1,2,3,4-tetrahydroisoquinoline, X4S06GK4KN, Isoquinoline, 1,2,3,4-tetrahydro-1-(phenylmethyl)-, CHEMBL21640, CHEBI:16804, S49 Isoquinoline, NSC-140739, Isoquinoline, 1-benzyl-1,2,3,4-tetrahydro-,, rac-(1R)-1-benzyl-1,2,3,4-tetrahydroisoquinoline, F0909-0437, UNII-X4S06GK4KN, AI3-61894, benzyltetrahydroisoquinoline, SCHEMBL4160731, SCHEMBL8332263, DTXSID70864898, SMSSF-0062146, BDBM50017041, MFCD00024130, NSC140739, SBB079136, AKOS005208313, AR-R 15209, HS-8834, HY-W029659, NSC 140739, J432.285A, 1-Benzyl-1,2,3,4-tetrahydroisoquinoline #, CS-0073683, NS00075503, C05201, EN300-120055, SR-01000009857, SR-01000009857-1, ISOQUINOLINE, 1-BENZYL-1,2,3,4-TETRAHYDRO-, Q27102081, ISOQUINOLINE,1,2,3,4-TETRAHYDRO-1-(PHENYLMETHYL)-

Application

1-Benzyl-1,2,3,4-tetrahydroisoquinoline serves as a key synthetic intermediate in the preparation of alkaloids and pharmacologically active compounds. Researchers utilize it in the development of central nervous system (CNS) targeting agents due to its structural similarity to natural isoquinoline derivatives. It is also employed in organic synthesis for constructing complex nitrogen-containing heterocycles. Its versatility makes it suitable for exploring structure-activity relationships in drug discovery.

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