Ethopabate

Base Information

Chemical Name:Ethopabate
CAS No.:59-06-3
Molecular Formula:C12H15NO4
Molecular Weight:237.255
Hs Code.:2924296000
European Community (EC) Number:200-414-3
UNII:F4X3L6068O
DSSTox Substance ID:DTXSID6046264
Nikkaji Number:J4.596I
Wikipedia:Ethopabate
Wikidata:Q5404419
NCI Thesaurus Code:C76420
ChEMBL ID:CHEMBL458769
Mol file:59-06-3.mol

Synonyms:Ethopabate

Suppliers and Price of Ethopabate

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

Usbiological
Ethopabate
250mg
$ 418.00

TRC
Ethopabate
250mg
$ 145.00

Sigma-Aldrich
Ethopabate United States Pharmacopeia (USP) Reference Standard
125 mg
$ 350.00

CSNpharm
Ethopabate
100mg
$ 48.00

CSNpharm
Ethopabate
25mg
$ 35.00

Crysdot
Methyl4-acetamido-2-ethoxybenzoate 95+%
100mg
$ 87.00

ChemScene
Ethopabate 99.42%
100mg
$ 60.00

ChemScene
Ethopabate 99.42%
500mg
$ 96.00

American Custom Chemicals Corporation
METHYL-4-ACETAMIDO-2-ETHOXYBENZOATE 95.00%
1G
$ 329.70

AK Scientific
Ethopabate
50mg
$ 38.00

Total 116 raw suppliers

Chemical Property of Ethopabate

Chemical Property:

Appearance/Colour:Colorless to yellow liquid
Vapor Pressure:1.82E-07mmHg at 25°C
Melting Point:148-151 °C
Refractive Index:1.545
Boiling Point:426.1 °C at 760 mmHg
PKA:14.12±0.70(Predicted)
Flash Point:211.5 °C
PSA：64.63000
Density:1.18 g/cm³
LogP:1.90330
Storage Temp.:0-6°C
XLogP3:1.2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:5
Exact Mass:237.10010796
Heavy Atom Count:17
Complexity:280

Purity/Quality:

99% ^*data from raw suppliers

Ethopabate ^*data from reagent suppliers

Safty Information:

Pictogram(s): Xn
Hazard Codes:Xn
Statements: 22

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

Canonical SMILES:CCOC1=C(C=CC(=C1)NC(=O)C)C(=O)OC
Uses A supplementary drug that improves the coccidiostatic effect of nicarbazin and amprolium in order to cure coccidiosis in chickens. antidepressant
Clinical Use Ethopabate is only a narrow anticoccidial spectrum drug against Eimeria acervulina. It has no or only slight activity against E. maxima, E. necatrix, E. tenella or E. brunetti. Today, ethopabate is applied only in combination with amprolium and sulfonamide.

Technology Process of Ethopabate

There total 6 articles about Ethopabate 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: 98.4%