2-Amino-3,5-dimethoxybenzoic acid

Base Information

Chemical Name:2-Amino-3,5-dimethoxybenzoic acid
CAS No.:79263-00-6
Molecular Formula:C9H11NO4
Molecular Weight:197.191
Hs Code.:
European Community (EC) Number:825-020-4
DSSTox Substance ID:DTXSID40511226
Wikidata:Q82369936

Synonyms:2-amino-3,5-dimethoxybenzoic acid;79263-00-6;Benzoic acid, 2-amino-3,5-dimethoxy-;SCHEMBL10579632;DTXSID40511226;2-amino-3,5-dimethoxybenzoicacid;MFCD12159987;AKOS010054995;AS-76703;CS-0199241;EN300-64831;D97525;A1-30079;Z234896241

Suppliers and Price of 2-Amino-3,5-dimethoxybenzoic acid

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 6 raw suppliers

Chemical Property of 2-Amino-3,5-dimethoxybenzoic acid

Chemical Property:

XLogP3:1.3
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:3
Exact Mass:197.06880783
Heavy Atom Count:14
Complexity:209

Purity/Quality:: 97% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=CC(=C(C(=C1)OC)N)C(=O)O

Technology Process of 2-Amino-3,5-dimethoxybenzoic acid

There total 7 articles about 2-Amino-3,5-dimethoxybenzoic acid 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: 69.0%

: 113884-71-2
Acide 2-nitro-3,5-dimethoxybenzoique

: 79263-00-6
2-amino-3,5-dimethoxybenzoic acid

Guidance literature:: With ammonia; iron(II) sulfate;

Reference yield: 14.0%

: 139617-15-5
ethyl 3-hydroxy-5,7-dimethoxy-2-oxo-2,3-dihydro-1H-indole-3-caboxylate

: 79263-00-6
2-amino-3,5-dimethoxybenzoic acid

: 76159-92-7
5,7-dimethoxyisatin

Guidance literature:: With sodium hydroxide; air; at 100 ℃; for 2.5h;

Reference yield:

: 76746-30-0
2-Nitro-3,5-dimethoxybenzoate de methyle

: 79263-00-6
2-amino-3,5-dimethoxybenzoic acid

Guidance literature:: Multi-step reaction with 2 steps

1: 28.6 g / H₂ / 5percent Pd/C / methanol; tetrahydrofuran / 46 h

2: 1 N NaOH / 2 h / Heating

With sodium hydroxide; hydrogen; palladium on activated charcoal; In tetrahydrofuran; methanol;
DOI:10.1021/jm00138a019