1,2,5,6,11,11b-Hexahydro-3H-indolizino[8,7-b]indol-3-one

Base Information

Chemical Name:1,2,5,6,11,11b-Hexahydro-3H-indolizino[8,7-b]indol-3-one
CAS No.:32283-51-5
Molecular Formula:C₁₄H₁₄N₂O
Molecular Weight:226.278
Hs Code.:
NSC Number:165211
Nikkaji Number:J361.888I
ChEMBL ID:CHEMBL3184054
Mol file:32283-51-5.mol

Synonyms:32283-51-5;NSC165211;1,2,5,6,11,11b-Hexahydro-3H-indolizino[8,7-b]indol-3-one;NSC 165211;MLS003106581;1,2,5,6,11,11b-Hexahydro-3H-indolizino(8,7-b)indol-3-one;1,2,5,6,11,11b-hexahydroindolizino[8,7-b]indol-3-one;CHEMBL3184054;QYILEJPKUMPTSA-UHFFFAOYSA-N;NSC-165211;2-Pyrrolidinone[1,5-c].beta.-carboline;SMR001821474;1,2,5,6,11,11b-Hexahydro-3H-indolizino[8,7-b]indol-3-one #;2,4,5,6,11,11b-hexahydro-1H-pyrrolo[5,1-a]beta-carbolin-3-one

Suppliers and Price of 1,2,5,6,11,11b-Hexahydro-3H-indolizino[8,7-b]indol-3-one

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 4 raw suppliers

Chemical Property of 1,2,5,6,11,11b-Hexahydro-3H-indolizino[8,7-b]indol-3-one

Chemical Property:

Vapor Pressure:2.36E-09mmHg at 25°C
Boiling Point:479.5°Cat760mmHg
Flash Point:243.8°C
Density:1.34g/cm³
XLogP3:1.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:0
Exact Mass:226.110613074
Heavy Atom Count:17
Complexity:343

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CC(=O)N2C1C3=C(CC2)C4=CC=CC=C4N3

Technology Process of 1,2,5,6,11,11b-Hexahydro-3H-indolizino[8,7-b]indol-3-one

There total 15 articles about 1,2,5,6,11,11b-Hexahydro-3H-indolizino[8,7-b]indol-3-one which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 84.0%

: 59048-75-8
N-[2-(1H-indol-3-yl)ethyl]pyrrolidine-2,5-dione

: 32283-51-5
1,2,5,6,11,11b-hexahydro-indolizino[8,7-b]indol-3-one

Guidance literature:: N-[2-(1H-indol-3-yl)ethyl]pyrrolidine-2,5-dione; With boron tribromide; In dichloromethane; at 20 ℃; for 12h; Molecular sieve; Inert atmosphere;

With sodium tetrahydroborate; In methanol; dichloromethane; for 0.5h; Molecular sieve; Inert atmosphere;
DOI:10.1007/s12039-015-0836-8

Reference yield: 82.0%

: 1311275-63-4
N-(2-(1H-indol-3-yl)ethyl)-N-allylacrylamide

: 32283-51-5
1,2,5,6,11,11b-hexahydro-indolizino[8,7-b]indol-3-one

Guidance literature:: With Hoveyda-Grubbs catalyst first generation; In m-xylene; for 24h; Inert atmosphere; Reflux;
DOI:10.1002/anie.201100417