Ethyl 6-bromoquinoline-2-carboxylate

Base Information

Chemical Name:Ethyl 6-bromoquinoline-2-carboxylate
CAS No.:1020572-61-5
Molecular Formula:C12H10BrNO2
Molecular Weight:280.121
Hs Code.:2933499090
DSSTox Substance ID:DTXSID70695422
Nikkaji Number:J3.139.913K
Wikidata:Q82624592
Mol file:1020572-61-5.mol

Synonyms:ETHYL 6-BROMOQUINOLINE-2-CARBOXYLATE;1020572-61-5;ethyl 6-bromo-2-quinolinecarboxylate;SCHEMBL2001591;DTXSID70695422;KIKGJVVDJNSJSQ-UHFFFAOYSA-N;AB65100;ETHYL6-BROMOQUINOLINE-2-CARBOXYLATE;FT-0711202;6-Bromoquinoline-2-carboxylic acid ethyl ester

Suppliers and Price of Ethyl 6-bromoquinoline-2-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

Labseeker
ethyl6-bromoquinoline-2-carboxylate 95
10g
$ 2108.00

Crysdot
Ethyl6-bromoquinoline-2-carboxylate 95+%
1g
$ 788.00

Chemenu
ethyl6-bromoquinoline-2-carboxylate 95%
1g
$ 745.00

American Custom Chemicals Corporation
ETHYL 6-BROMOQUINOLINE-2-CARBOXYLATE 95.00%
5MG
$ 502.45

Total 4 raw suppliers

Chemical Property of Ethyl 6-bromoquinoline-2-carboxylate

Chemical Property:

Boiling Point:385.2±22.0 °C(Predicted)
PKA:1.18±0.43(Predicted)
PSA：39.19000
Density:1.495±0.06 g/cm3(Predicted)
LogP:3.17400
XLogP3:3.4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:278.98949
Heavy Atom Count:16
Complexity:259

Purity/Quality:

98%min ^*data from raw suppliers

ethyl6-bromoquinoline-2-carboxylate 95 ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCOC(=O)C1=NC2=C(C=C1)C=C(C=C2)Br

Technology Process of Ethyl 6-bromoquinoline-2-carboxylate

There total 4 articles about Ethyl 6-bromoquinoline-2-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: 80.0%

: 2235-00-9,25189-83-7
vinylcaprolactam

: 915712-34-4
(4-bromo-phenylimino)-acetic acid ethyl ester

: 1020572-61-5
ethyl 6-bromo-2-quinolinecarboxylate

Guidance literature:: With tris(p-bromophenylammoniumyl) hexachloroantimonate; In 1,2-dichloro-ethane; Reflux;
DOI:10.1016/j.tetlet.2012.10.097

Reference yield: 67.0%

: 877-42-9
6-Bromo-2-methyl-quinoline

: 64-17-5
ethanol

: 1020572-61-5
ethyl 6-bromo-2-quinolinecarboxylate

Guidance literature:: With copper(l) iodide; 1,10-Phenanthroline; diphenyl-phosphinic acid; oxygen; In 1,4-dioxane; at 120 ℃; for 24h; under 760.051 Torr;
DOI:10.1039/c5cy02069g