2-Hydroxy-4-methoxy-3-methylbenzoic acid

Base Information

Chemical Name:2-Hydroxy-4-methoxy-3-methylbenzoic acid
CAS No.:116371-82-5
Molecular Formula:C9H10O4
Molecular Weight:182.176
Hs Code.:
European Community (EC) Number:893-091-9
Mol file:116371-82-5.mol

Synonyms:2-hydroxy-4-methoxy-3-methylbenzoic acid;116371-82-5;SCHEMBL4143348

Suppliers and Price of 2-Hydroxy-4-methoxy-3-methylbenzoic 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
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Total 1 raw suppliers

Chemical Property of 2-Hydroxy-4-methoxy-3-methylbenzoic acid

Chemical Property:

XLogP3:2
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:2
Exact Mass:182.05790880
Heavy Atom Count:13
Complexity:192

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=C(C=CC(=C1O)C(=O)O)OC

Technology Process of 2-Hydroxy-4-methoxy-3-methylbenzoic acid

There total 10 articles about 2-Hydroxy-4-methoxy-3-methylbenzoic 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:

: 331816-06-9
2',7-dimethoxy-8-methylisoflavone

: 116371-82-5
2-hydroxy-4-methoxy-3-methylbenzoic acid

: 579-75-9
2-Methoxybenzoic acid

Guidance literature:: 2',7-dimethoxy-8-methylisoflavone; Alkaline hydrolysis;

With hydroxide; dihydrogen peroxide;

Reference yield:

: 7-hydroxy-8-methyl-2'-methoxyisoflavone

: 116371-82-5
2-hydroxy-4-methoxy-3-methylbenzoic acid

Guidance literature:: Multi-step reaction with 2 steps

1.1: K₂CO₃ / acetone / 10 h / Heating

2.1: Alkaline hydrolysis

2.2: H₂O₂; OH^(1-)

With potassium carbonate; In acetone;

Reference yield:

: 7-O-acetyl-8-methyl-2'-methoxyisoflavone

: 116371-82-5
2-hydroxy-4-methoxy-3-methylbenzoic acid

Guidance literature:: Multi-step reaction with 3 steps

1.1: 110 mg / H₂SO₄ / methanol / 1 h

2.1: K₂CO₃ / acetone / 10 h / Heating

3.1: Alkaline hydrolysis

3.2: H₂O₂; OH^(1-)

With sulfuric acid; potassium carbonate; In methanol; acetone;