2-Chloro-3-(2-chloroethyl)-4-methylquinoline

Base Information

Chemical Name:2-Chloro-3-(2-chloroethyl)-4-methylquinoline
CAS No.:62595-01-1
Molecular Formula:C₁₂H₁₁Cl₂N
Molecular Weight:240.132
Hs Code.:
DSSTox Substance ID:DTXSID90500504
Wikidata:Q82352149

Synonyms:2-Chloro-3-(2-chloroethyl)-4-methylquinoline;62595-01-1;DTXSID90500504

Suppliers and Price of 2-Chloro-3-(2-chloroethyl)-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

Total 1 raw suppliers

Chemical Property of 2-Chloro-3-(2-chloroethyl)-4-methylquinoline

Chemical Property:

XLogP3:4.4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:2
Exact Mass:239.0268547
Heavy Atom Count:15
Complexity:210

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=C(C(=NC2=CC=CC=C12)Cl)CCCl

Technology Process of 2-Chloro-3-(2-chloroethyl)-4-methylquinoline

There total 3 articles about 2-Chloro-3-(2-chloroethyl)-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:

: 5970-94-5
2-(2-hydroxy-4-methyl-[3]quinolyl)-ethanol

: 62595-01-1
2-Chlor-3-(2-chlorethyl)-4-methylchinolin

Guidance literature:: With trichlorophosphate; at 125 ℃;

Reference yield:

: 107516-65-4
(2-hydroxy-4-methyl-[3]quinolyl)-acetic acid ethyl ester

: 62595-01-1
2-Chlor-3-(2-chlorethyl)-4-methylchinolin

Guidance literature:: Multi-step reaction with 2 steps

1: diethyl ether; lithium alanate

2: phosphoryl chloride / 125 °C

With lithium aluminium tetrahydride; diethyl ether; trichlorophosphate;