CAS 1447606-51-0

1a,2,3,7b-Tetrahydro-1H-cyclopropa[c]quinoline

Description:

1a,2,3,7b-Tetrahydro-1H-cyclopropa[c]quinoline is a bicyclic organic compound characterized by its unique fused ring structure, which includes a cyclopropane and a quinoline moiety. This compound typically exhibits a molecular formula that reflects its complex structure, contributing to its potential biological activity. It is a colorless to pale yellow liquid or solid, depending on the specific conditions and purity. The presence of nitrogen in the quinoline ring suggests that it may participate in hydrogen bonding and exhibit basic properties. Its stereochemistry can influence its reactivity and interactions with biological targets, making it of interest in medicinal chemistry. The compound may also display interesting pharmacological properties, which could be explored in drug development. However, detailed studies on its toxicity, solubility, and stability are essential for understanding its practical applications. As with many nitrogen-containing heterocycles, it may also be involved in various chemical reactions, including electrophilic substitutions and cycloadditions, further expanding its utility in synthetic organic chemistry.

Formula: C₁₀H₁₁N

InChI: InChI=1S/C10H11N/c1-2-4-10-8(3-1)9-5-7(9)6-11-10/h1-4,7,9,11H,5-6H2

InChI key: InChIKey=OEHUSLVNUHYNLQ-UHFFFAOYSA-N

SMILES: C12C=3C(NCC1C2)=CC=CC3

Synonyms:

• 1a,2,3,7b-Tetrahydro-1H-cyclopropa[c]quinoline
• 1H-Cyclopropa[c]quinoline, 1a,2,3,7b-tetrahydro-

1A,2,3,7B-TETRAHYDRO-1H-CYCLOPROPA[C]QUINOLINE

CAS: 1447606-51-0

Purity: 95.0%

Molecular weight: 145.2050018310547

Ref: 10-F334318