Quindoline

Base Information

Chemical Name:Quindoline
CAS No.:243-58-3
Molecular Formula:C15H10 N2
Molecular Weight:218.258
Hs Code.:
NSC Number:647766,177394
DSSTox Substance ID:DTXSID70179030
Nikkaji Number:J454.491I,J483.529H
Wikidata:Q6095002,Q104667337
Metabolomics Workbench ID:127465
ChEMBL ID:CHEMBL224248
Mol file:243-58-3.mol

Synonyms:quindoline

Suppliers and Price of Quindoline

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 10 raw suppliers

Chemical Property of Quindoline

Chemical Property:

Vapor Pressure:1.71E-08mmHg at 25°C
Melting Point:247～248℃
Boiling Point:468.2°Cat760mmHg
PKA:15.20±0.30(Predicted)
Flash Point:217.5°C
PSA：28.68000
Density:1.336g/cm³
LogP:3.86930
XLogP3:3.4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:0
Exact Mass:218.084398327
Heavy Atom Count:17
Complexity:291

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C2C(=C1)C=C3C(=N2)C4=CC=CC=C4N3

Technology Process of Quindoline

There total 5 articles about Quindoline 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: 90.0%

: 250593-14-7
2'-(3-bromoquinolin-2-yl)aniline

: 243-58-3
quindoline

: 29184-58-5
2-(2-aminophenyl)quinoline

Guidance literature:: With potassium tert-butylate; In dimethyl sulfoxide; at 20 ℃; for 6h; Inert atmosphere; Irradiation;
DOI:10.1039/c9nj01961h

Reference yield: 45.0%

: 848086-11-3
N-(2-bromophenyl)quinolin-3-amine

: 243-58-3
quindoline

: 108618-27-5
N-phenylquinolin-3-ylamine

: 205-32-3
3,4-benzo-β-carboline

Guidance literature:: With sodium acetate; bis-triphenylphosphine-palladium(II) chloride; In N,N-dimethyl acetamide; at 130 ℃; for 48h;
DOI:10.1016/j.tet.2004.11.073