7-Bromo-2-chloro-4-methylquinoline

Base Information

Chemical Name:7-Bromo-2-chloro-4-methylquinoline
CAS No.:89446-52-6
Molecular Formula:C10H7BrClN
Molecular Weight:256.52600
Hs Code.:2933499090
DSSTox Substance ID:DTXSID40561766
Nikkaji Number:J2.021.091E
Wikidata:Q82445626
Mol file:89446-52-6.mol

Synonyms:7-bromo-2-chloro-4-methylquinoline;89446-52-6;Quinoline, 7-bromo-2-chloro-4-methyl-;MFCD21647757;2-chloro-4-methyl-7-bromoquinoline;SCHEMBL7424524;DTXSID40561766;FCQMZVFGSMJLPM-UHFFFAOYSA-N;7-bromo-2-chloro-4-methyl-quinoline;AKOS016353043;CS-0280163;G74711;EN300-1197928;A929571

Suppliers and Price of 7-Bromo-2-chloro-4-methylquinoline

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

SynQuest Laboratories
7-Bromo-2-chloro-4-methylquinoline
1 g
$ 400.00

Total 4 raw suppliers

Chemical Property of 7-Bromo-2-chloro-4-methylquinoline

Chemical Property:

PSA：12.89000
LogP:3.95910
XLogP3:4.2
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:0
Exact Mass:254.94504
Heavy Atom Count:13
Complexity:188

Purity/Quality:

99% ^*data from raw suppliers

7-Bromo-2-chloro-4-methylquinoline ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:
Statements: 41
Safety Statements: 26-39

MSDS Files:

Useful:

Canonical SMILES:CC1=CC(=NC2=C1C=CC(=C2)Br)Cl

Technology Process of 7-Bromo-2-chloro-4-methylquinoline

There total 3 articles about 7-Bromo-2-chloro-4-methylquinoline 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: 71.0%

: 89446-51-5
7-bromo-4-methyl-1,2-dihydroquinolin-2-one

: 89446-52-6
7-bromo-2-chloro-4-methyl-quinoline

Guidance literature:: With trichlorophosphate; for 2h; Heating;
DOI:10.1021/jm00128a041

Reference yield:

: 89446-51-5
7-bromo-4-methyl-quinolin-2-ol

: 89446-52-6
7-bromo-2-chloro-4-methyl-quinoline

Guidance literature:: In ethanol; trichlorophosphate;

Reference yield:

: 61579-06-4
N-(3-bromo-phenyl)-3-oxo-butyramide

: 89446-52-6
7-bromo-2-chloro-4-methyl-quinoline

Guidance literature:: Multi-step reaction with 2 steps

1: 84 percent / conc. H₂SO₄ / 1.5 h / 120 °C

2: 71 percent / POCl₃ / 2 h / Heating

With sulfuric acid; trichlorophosphate;
DOI:10.1021/jm00128a041