Ethyl 6-bromo-2-methylquinoline-4-carboxylate

Base Information

Chemical Name:Ethyl 6-bromo-2-methylquinoline-4-carboxylate
CAS No.:62482-30-8
Molecular Formula:C13H12BrNO2
Molecular Weight:294.14
Hs Code.:
NSC Number:201886
DSSTox Substance ID:DTXSID20308070
Nikkaji Number:J3.624.733I
Wikidata:Q82055743
Mol file:62482-30-8.mol

Synonyms:ethyl 6-bromo-2-methylquinoline-4-carboxylate;62482-30-8;NSC201886;Maybridge1_000196;Oprea1_425652;SCHEMBL5810083;HMS542A20;DTXSID20308070;CCG-51710;MFCD00115248;NSC-201886;MS-21963;FT-0757049;J-521174;SR-01000640996-1;ethyl 6-bromo-2-methylquinoline-4-carboxylate, AldrichCPR

Suppliers and Price of Ethyl 6-bromo-2-methylquinoline-4-carboxylate

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

American Custom Chemicals Corporation
ETHYL 6-BROMO-2-METHYLQUINOLINE-4-CARBOXYLATE 95.00%
10G
$ 1574.15

American Custom Chemicals Corporation
ETHYL 6-BROMO-2-METHYLQUINOLINE-4-CARBOXYLATE 95.00%
1G
$ 194.58

Total 10 raw suppliers

Chemical Property of Ethyl 6-bromo-2-methylquinoline-4-carboxylate

Chemical Property:

Vapor Pressure:6.1E-06mmHg at 25°C
Melting Point:110oC
Boiling Point:378.9°C at 760 mmHg
PKA:2.88±0.50(Predicted)
Flash Point:182.9°C
PSA：39.19000
Density:1.444g/cm³
LogP:3.48240
XLogP3:3.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:293.00514
Heavy Atom Count:17
Complexity:285

Purity/Quality:

98%min ^*data from raw suppliers

ETHYL 6-BROMO-2-METHYLQUINOLINE-4-CARBOXYLATE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCOC(=O)C1=C2C=C(C=CC2=NC(=C1)C)Br

Technology Process of Ethyl 6-bromo-2-methylquinoline-4-carboxylate

There total 4 articles about Ethyl 6-bromo-2-methylquinoline-4-carboxylate 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: 85.0%

: 37509-21-0
6-bromo-2-methylquinoline-4-carboxylic acid

: 64-17-5
ethanol

: 62482-30-8
ethyl 6-bromo-2-methylquinoline-4-carboxylate

Guidance literature:: With sulfuric acid; for 15h; Reflux;
DOI:10.1002/ardp.201900086

Reference yield: 65.0%

: 88912-02-1
ethyl 2-(4-bromophenylamino)propanoate

: 62482-30-8
ethyl 6-bromo-2-methylquinoline-4-carboxylate

Guidance literature:: With boron trifluoride diethyl etherate; oxygen; tris(p-bromophenylammoniumyl) hexachloroantimonate; In 1,2-dichloro-ethane; at 60 ℃;
DOI:10.1039/c7ob00446j