2-Methoxybenzoate

Base Information

• Chemical Name: 2-Methoxybenzoate
• CAS No.: 16887-70-0
• Molecular Formula: C₈H₇O₃
• Molecular Weight: 151.142
• DSSTox Substance ID: DTXSID001299870
• Nikkaji Number: J2.343.726K
• Wikidata: Q27126477

Synonyms:2-methoxybenzoate;2-methoxybenzoic acid;2-methoxybenzoic acid, sodium salt;o-anisic acid;o-methoxybenzoic acid

Chemical Property of 2-Methoxybenzoate

Chemical Property:

• XLogP3: 2.2
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 1
• Exact Mass: 151.039519081
• Heavy Atom Count: 11
• Complexity: 139

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: COC1=CC=CC=C1C(=O)[O-]

Technology Process of 2-Methoxybenzoate

There total 1 articles about 2-Methoxybenzoate 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:

2-Methoxy-thiobenzoic acid S-(2,4-dinitro-phenyl) ester (83280-97-1) → 2,4-dinitrobenzenethiolate anion (56437-88-8) + o-methoxybenzoic acid anion (16887-70-0)

Guidance literature:

With hydroxide; In 1,4-dioxane; water; Kinetics; Thermodynamic data; Mechanism; pH 9.22, logarithms of the rate constants, ΔH(excit.), ΔS(excit.);

DOI:10.1007/BF00954149

Reference yield:

o-methoxybenzoic acid anion (16887-70-0) + cobalt(II) nitrate → Co(2+)*C8H7O3(1-)=Co(C8H7O3)(1+)

Guidance literature:

In nitric acid; Electrochem. Process; 35°C, I=0.1 M; ionophoretic reactn. conditions, 200 V D.C.;

Reference yield:

o-methoxybenzoic acid anion (16887-70-0) + nickel(II) nitrate → Ni(2+)*C8H7O3(1-)=Ni(C8H7O3)(1+)

Guidance literature:

In nitric acid; Electrochem. Process; 35°C, I=0.1 M; ionophoretic reactn. conditions, 200 V D.C.;

upstream raw materials:

2-Methoxy-thiobenzoic acid S-(2,4-dinitro-phenyl) ester

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