Ethyl 2-(2-bromophenyl)-2-oxoacetate

Base Information

Chemical Name:Ethyl 2-(2-bromophenyl)-2-oxoacetate
CAS No.:62123-82-4
Molecular Formula:C10H9BrO3
Molecular Weight:257.084
Hs Code.:2918300090
DSSTox Substance ID:DTXSID60482540
Nikkaji Number:J3.614.843H
Wikidata:Q82318965

Synonyms:Ethyl 2-(2-bromophenyl)-2-oxoacetate;62123-82-4;2-Bromo-oxo-benzeneacetic acid ethyl ester;SCHEMBL16039556;DTXSID60482540;ODUHAMLUWOLQKF-UHFFFAOYSA-N;MFCD22552906;Ethyl2-(2-bromophenyl)-2-oxoacetate

Suppliers and Price of Ethyl 2-(2-bromophenyl)-2-oxoacetate

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

Crysdot
Ethyl2-(2-bromophenyl)-2-oxoacetate 95+%
10g
$ 700.00

Crysdot
Ethyl2-(2-bromophenyl)-2-oxoacetate 95+%
5g
$ 465.00

Crysdot
Ethyl2-(2-bromophenyl)-2-oxoacetate 95+%
25g
$ 937.00

Crysdot
Ethyl2-(2-bromophenyl)-2-oxoacetate 95+%
100g
$ 2352.00

Alichem
Ethyl2-(2-bromophenyl)-2-oxoacetate
100g
$ 1881.00

Alichem
Ethyl2-(2-bromophenyl)-2-oxoacetate
25g
$ 767.60

Acrotein
2-Bromo-oxo-benzeneaceticacidethylester 97%
1g
$ 265.83

Total 6 raw suppliers

Chemical Property of Ethyl 2-(2-bromophenyl)-2-oxoacetate

Chemical Property:

PSA：43.37000
LogP:2.19490
XLogP3:2.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:4
Exact Mass:255.97351
Heavy Atom Count:14
Complexity:227

Purity/Quality:

99% ^*data from raw suppliers

Ethyl2-(2-bromophenyl)-2-oxoacetate 95+% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCOC(=O)C(=O)C1=CC=CC=C1Br

Technology Process of Ethyl 2-(2-bromophenyl)-2-oxoacetate

There total 5 articles about Ethyl 2-(2-bromophenyl)-2-oxoacetate 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%

: 64-17-5
ethanol

: 26767-16-8
2-(2-bromophenyl)-2-oxoacetic acid

: 62123-82-4
ethyl 2-(2-bromophenyl)-2-oxoacetate

Guidance literature:: With thionyl chloride; at 80 ℃; for 12h;

Reference yield: 70.0%

: 50671-05-1
3-(2-bromophenyl)-3-oxopropionic acid ethyl ester

: 62123-82-4
ethyl 2-(2-bromophenyl)-2-oxoacetate

Guidance literature:: With 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; acetic acid; copper(I) bromide; at 100 ℃;
DOI:10.1039/c7ob00241f

Reference yield: 55.0%

: 64-17-5
ethanol

: 2142-69-0
2-bromophenyl methyl ketone

: 62123-82-4
ethyl 2-(2-bromophenyl)-2-oxoacetate

Guidance literature:: With 2,2,6,6-tetramethyl-piperidine; 4-nitro-phenol; oxygen; potassium iodide; for 11.5h; Electrochemical reaction;
DOI:10.1002/chem.201302307