Ethyl 3-bromo-4-isopropoxybenzoate

Base Information

Chemical Name:Ethyl 3-bromo-4-isopropoxybenzoate
CAS No.:860695-52-9
Molecular Formula:C₁₂H₁₅BrO₃
Molecular Weight:287.153
Hs Code.:2918990090
DSSTox Substance ID:DTXSID70474259
Wikidata:Q82304139
Mol file:860695-52-9.mol

Synonyms:ethyl 3-bromo-4-isopropoxybenzoate;860695-52-9;ethyl 3-bromo-4-propan-2-yloxybenzoate;Ethyl3-bromo-4-isopropoxybenzoate;3-bromo-4-propan-2-yloxybenzoic acid ethyl ester;AN-329/43341714;SCHEMBL16605593;DTXSID70474259;AKOS000501741;ethyl 3-bromanyl-4-propan-2-yloxy-benzoate;CS-0361513;FT-0652793;A841549

Suppliers and Price of Ethyl 3-bromo-4-isopropoxybenzoate

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
Ethyl3-bromo-4-isopropoxybenzoate 97%
1g
$ 510.00

Aronis compounds
ethyl3-bromo-4-isopropoxybenzoate
5mg
$ 15.00

American Custom Chemicals Corporation
ETHYL 3-BROMO-4-ISOPROPOXYBENZOATE 95.00%
0.25G
$ 482.00

American Custom Chemicals Corporation
ETHYL 3-BROMO-4-ISOPROPOXYBENZOATE 95.00%
5G
$ 2246.48

Alichem
Ethyl3-bromo-4-isopropoxybenzoate
1g
$ 663.00

Total 20 raw suppliers

Chemical Property of Ethyl 3-bromo-4-isopropoxybenzoate

Chemical Property:

PSA：35.53000
LogP:3.41300
Storage Temp.:2-8°C
XLogP3:3.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:5
Exact Mass:286.02046
Heavy Atom Count:16
Complexity:230

Purity/Quality:

97% ^*data from raw suppliers

Ethyl3-bromo-4-isopropoxybenzoate 97% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCOC(=O)C1=CC(=C(C=C1)OC(C)C)Br

Technology Process of Ethyl 3-bromo-4-isopropoxybenzoate

There total 3 articles about Ethyl 3-bromo-4-isopropoxybenzoate 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: 65.0%

: 122488-52-2
ethyl 4-isopropoxybenzoate

: 860695-52-9
3-bromo-4-isopropoxy-benzoic acid ethyl ester

Guidance literature:: With bromine; In dichloromethane; at -10 - 40 ℃; for 3.5h;

Reference yield:

: 99-96-7
4-hydroxy-benzoic acid

: 860695-52-9
3-bromo-4-isopropoxy-benzoic acid ethyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: sulfuric acid / 8 h / Reflux

2: potassium carbonate / ethanol / 2 h / 60 °C

3: bromine / dichloromethane / 3.5 h / -10 - 40 °C

With sulfuric acid; bromine; potassium carbonate; In ethanol; dichloromethane;

Reference yield:

: 120-47-8
Ethyl 4-hydroxybenzoate

: 860695-52-9
3-bromo-4-isopropoxy-benzoic acid ethyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: potassium carbonate / ethanol / 2 h / 60 °C

2: bromine / dichloromethane / 3.5 h / -10 - 40 °C

With bromine; potassium carbonate; In ethanol; dichloromethane;