8a-(5-vinyl-1-azabicyclo[2.2.2]oct-2-yl)-2,3,8,8a-tetrahydro-3aH-furo[2,3-b]indol-3a-ol

Quality products?make an important contribution to long-term revenue and profitability. Factory supply 8a-(5-vinyl-1-azabicyclo[2.2.2]oct-2-yl)-2,3,8,8a-tetrahydro-3aH-furo[2,3-b]indol-3a-ol 464-85-7 with sufficient stock and high standard

1.What is the 8a-(5-vinyl-1-azabicyclo[2.2.2]oct-2-yl)-2,3,8,8a-tetrahydro-3aH-furo[2,3-b]indol-3a-ol ?

8a-(5-vinyl-1-azabicyclo[2.2.2]oct-2-yl)-2,3,8,8a-tetrahydro-3aH-furo[2,3-b]indol-3a-ol is a complex organic compound characterized by a unique fused ring system. It features a furo[2,3-b]indole ring fused with a bicyclic azabicyclooctane, and it contains a vinyl group at the 5th position of the azabicyclooctane ring. Additionally, a hydroxyl group is present at the 3a position of the furo[2,3-b]indole ring. This intricate molecular architecture suggests that the compound may possess a range of biological activities, making it a promising candidate for further exploration in medicinal and pharmacological research.

2.What is the CAS number for 8a-(5-vinyl-1-azabicyclo[2.2.2]oct-2-yl)-2,3,8,8a-tetrahydro-3aH-furo[2,3-b]indol-3a-ol ?

The CAS number of 8a-(5-vinyl-1-azabicyclo[2.2.2]oct-2-yl)-2,3,8,8a-tetrahydro-3aH-furo[2,3-b]indol-3a-ol is 464-85-7.

3.What are another words for 8a-(5-vinyl-1-azabicyclo[2.2.2]oct-2-yl)-2,3,8,8a-tetrahydro-3aH-furo[2,3-b]indol-3a-ol ?

Synonyms?for?8a-(5-vinyl-1-azabicyclo[2.2.2]oct-2-yl)-2,3,8,8a-tetrahydro-3aH-furo[2,3-b]indol-3a-ol 464-85-7:3aH-Furo[2,3-b]indol-3a-ol,8a-(5-ethenyl-1-azabicyclo[2.2.2]oct-2-yl)-2,3,8,8a-tetrahydro-, [1S-[1a,2a(3aS*,8aR*),4a,5b]]-; Quinamine (7CI); Alkaloid B from Cinchona ledgeriana

4.What is 8a-(5-vinyl-1-azabicyclo[2.2.2]oct-2-yl)-2,3,8,8a-tetrahydro-3aH-furo[2,3-b]indol-3a-ol (464-85-7) used for?

Used in Medicinal Chemistry:
8a-(5-vinyl-1-azabicyclo[2.2.2]oct-2-yl)-2,3,8,8a-tetrahydro-3aH-furo[2,3-b]indol-3a-ol is used as a lead compound for the development of new drugs due to its complex structure and potential for biological activity. Its unique molecular features may allow it to interact with various biological targets, offering opportunities for the treatment of a range of diseases.
Used in Pharmacological Research:
In the field of pharmacology, 8a-(5-vinyl-1-azabicyclo[2.2.2]oct-2-yl)-2,3,8,8a-tetrahydro-3aH-furo[2,3-b]indol-3a-ol is utilized as a subject of study to understand its interactions with biological systems. Researchers are interested in exploring its potential effects on cellular processes and its ability to modulate specific signaling pathways, which could lead to the discovery of novel therapeutic agents.
Used in Drug Design and Optimization:
8a-(5-vinyl-1-azabicyclo[2.2.2]oct-2-yl)-2,3,8,8a-tetrahydro-3aH-furo[2,3-b]indol-3a-ol serves as a starting point for drug design and optimization efforts. Its structural features can be modified to enhance its pharmacological properties, such as potency, selectivity, and bioavailability, ultimately leading to the creation of more effective and safer medications.
Used in Chemical Synthesis:
In the realm of chemical synthesis, 8a-(5-vinyl-1-azabicyclo[2.2.2]oct-2-yl)-2,3,8,8a-tetrahydro-3aH-furo[2,3-b]indol-3a-ol is employed as a building block or intermediate in the synthesis of more complex molecules. Its unique structure can be further elaborated upon to create a variety of novel compounds with potential applications in various fields, including materials science and specialty chemicals.

InChI:InChI=1/C19H24N2O2/c1-2-13-12-21-9-7-14(13)11-17(21)19-18(22,8-10-23-19)15-5-3-4-6-16(15)20-19/h2-6,13-14,17,20,22H,1,7-12H2/t13-,14-,17-,18?,19?/m0/s1

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