Ethyl 3-bromo-1,2-oxazole-4-carboxylate

Base Information

Chemical Name:Ethyl 3-bromo-1,2-oxazole-4-carboxylate
CAS No.:111303-36-7
Molecular Formula:C6H6BrNO3
Molecular Weight:
Hs Code.:
European Community (EC) Number:839-701-9
ChEMBL ID:CHEMBL4578185
DSSTox Substance ID:DTXSID90549892
Wikidata:Q82429083

Synonyms:111303-36-7;Ethyl 3-bromo-1,2-oxazole-4-carboxylate;Ethyl 3-bromoisoxazole-4-carboxylate;4-Isoxazolecarboxylic acid, 3-bromo-, ethyl ester;CHEMBL4578185;DTXSID90549892;AT19726;Ethyl3-bromo-1,2-oxazole-4-carboxylate;EN300-250524

Suppliers and Price of Ethyl 3-bromo-1,2-oxazole-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

Total 2 raw suppliers

Chemical Property of Ethyl 3-bromo-1,2-oxazole-4-carboxylate

Chemical Property:

XLogP3:1.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:3
Exact Mass:218.95311
Heavy Atom Count:11
Complexity:153

Purity/Quality:: 98%min ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCOC(=O)C1=CON=C1Br

Technology Process of Ethyl 3-bromo-1,2-oxazole-4-carboxylate

There total 1 articles about Ethyl 3-bromo-1,2-oxazole-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:

: 74213-24-4
N-dibromomethylidenehydroxylamine

: 623-47-2
propynoic acid ethyl ester

: 105174-97-8
3-Bromo-5-isoxazolecarboxylic Acid Ethyl Ester

: 111303-36-7
3-Bromo-4-isoxazolecarboxylic Acid Ethyl Ester

Guidance literature:: With potassium hydrogencarbonate; In water; ethyl acetate; added dropwise during 6 h at r.t., then stirring 18 h;
DOI:10.1002/jhet.5570240109