6H-Cyclopropa[g]quinoline

Base Information

Chemical Name:6H-Cyclopropa[g]quinoline
CAS No.:130566-12-0
Molecular Formula:C₁₀H₇N
Molecular Weight:141.172
Hs Code.:
DSSTox Substance ID:DTXSID70563031
Wikidata:Q82447373
Mol file:130566-12-0.mol

Synonyms:6H-Cyclopropa[g]quinoline;130566-12-0;6H-Cyclopropa[g]quinoline(9CI);DTXSID70563031;AKOS006373444

Suppliers and Price of 6H-Cyclopropa[g]quinoline

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 2 raw suppliers

Chemical Property of 6H-Cyclopropa[g]quinoline

Chemical Property:

PSA：12.89000
LogP:2.13900
XLogP3:0.4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:0
Exact Mass:141.057849228
Heavy Atom Count:11
Complexity:166

Purity/Quality:: 85.0-99.8% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1C2=C1C=C3C(=C2)C=CC=N3

Technology Process of 6H-Cyclopropa[g]quinoline

There total 2 articles about 6H-Cyclopropa[g]quinoline 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: 82.0%

: 130566-11-9
1-bromo-7a-chloro-1a,2,7,7a-tetrahydrocyclopropaquinoline

: 130566-12-0
1H-cyclopropaquinoline

Guidance literature:: With potassium tert-butylate; In tetrahydrofuran; at -78 ℃; for 3h;
DOI:10.1002/hlca.19900730512

Reference yield:

: 83781-67-3
trimethyl<<2-<(trimethylsilyl)methyl>pyridin-3-yl>methyl>ammonium bromide

: 130566-12-0
1H-cyclopropaquinoline

Guidance literature:: Multi-step reaction with 2 steps

2: 82 percent / t-BuOK / tetrahydrofuran / 3 h / -78 °C

With potassium tert-butylate; In tetrahydrofuran;
DOI:10.1002/hlca.19900730512