103259-06-9

Usage

Uses

Used in Chemical Synthesis:
2-Amino-6-methoxycarbonyl benzoic acid is used as a key intermediate in the synthesis of various complex organic molecules. Its functional groups allow for multiple reaction pathways, making it a valuable building block in the creation of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-Amino-6-methoxycarbonyl benzoic acid is used as a starting material for the development of new drugs. Its versatile structure enables the design of molecules with specific therapeutic properties, targeting a wide range of medical conditions.
Used in Agrochemical Industry:
2-Amino-6-methoxycarbonyl benzoic acid is employed as a precursor in the synthesis of agrochemicals, such as pesticides and herbicides. Its reactivity and functional groups contribute to the creation of effective compounds for agricultural applications.
Used in Material Science:
In material science, 2-Amino-6-methoxycarbonyl benzoic acid is used as a component in the development of advanced materials, such as polymers and composites. Its functional groups can be utilized to create materials with tailored properties, such as improved strength, flexibility, or thermal stability.

Upstream product

• 603-11-2 3-nitrophthalic acid 
• 67-56-1 methanol 
• 5434-20-8 3-aminophthalic acid 
• 641-70-3 3-nitrophthalic acid anhydride 
• 21606-04-2 methyl 2-carboxy-3-nitrobenzoate 

Downstream Products

• 141344-48-1 methyl 2-carboxy-3-<<2-(4-carboxymethyl)imidazolyl>azo>benzoate 
• 99-05-8 meta-aminobenzoic acid 
• 103259-25-2 N,N',N''-tris(4-methylphenyl)-1,8,16-triptycenetricarboxamide 
• 103259-26-3 N,N',N''-tris(4-hydroxyphenyl)-1,8,13-triptycenetricarboxamide 
• 1326304-06-6 9-phenyl-5H-anthro[9,1-jk]fluoranthen-5-one 
• 1326304-04-4 1,2-bis(4-methoxyphenyl)-3-phenyl-7H-benz[de]anthracen-7-one 
• 1326304-03-3 1,2,3-triphenyl-7H-benzo[de]anthracen-7-one 
• 136131-56-1 2-benzyl-8-carbomethoxy-1-naphthol 
• 136131-61-8 2-benzyl-5-carbomethoxy-1-naphthol 

Relevant academic research and scientific papers

Method for preparing dimethyl acetamidophthalate

The invention relates to a method for preparing dimethyl acetamidophthalate. The method comprises the following steps: dissolving nitrophthalic anhydride in methanol, adding a graphite-phase carbon nitride supported cuprous catalyst (g-C3N4/Cu2O) and acetic anhydride, and carrying out reacting to obtain dimethyl acetamidophthalate. 200-300 mg of the graphite-phase carbon nitride supported cuprouscatalyst (g-C3N4/Cu2O) is used for every millimole of nitrophthalic anhydride, and 2.0-3.0 mmol of acetic anhydride is used for every millimole of nitrophthalic anhydride.

Preparation method for 3-aminophthalic acid and derivative thereof

The invention discloses a preparation method for an apremilast intermediate, i.e., 3-aminophthalic acid, and a derivative thereof. The preparation method comprises a step of reducing 3-nitrophthalic acid or a derivative thereof in the presence of a reducing agent selected from a group consisting of elemental sulfur, sulfide and a mixture of elemental sulfur and sulfide. The method has the advantages of high yield, simple operation, environmental protection and suitability for industrial production.

3, 4-DI-SUBSTITUTED CYCLOBUTENE- 1, 2 -DIONES AS CXCR2 RECEPTOR ANTAGONISTS

The present invention relates to compounds of formula (I) wherein R1, R2, Ar, p, R4 and R5 are as defined herein, which are useful for creating diseases which respond to CXCR2 receptor mediators. Pharmaceutical

BICYCLIC ARYL AND HETEROARYL COMPOUNDS FOR THE TREATMENT OF METABOLIC DISORDERS

Compounds of formula (I): or pharmaceutically acceptable salts thereof, are opioid receptor modulators, e.g. mu- opioid receptor antagonists, neutral antagonists or inverse agonists, and are useful for the treatment of metabolic disorders including obesity.

Comparable rates for cleavage of amide and ester bonds through nucleophilic attack by carboxylate anion and general acid catalysis by metal-bound water in a carboxypeptidase a model

The kinetics of the Cu(II)- or Ni(II)-catalyzed deacylation of the methtyl ester (3) and the N,N-dimethyl amide (4) of 2-carboxy-6-[[2-(4-carboxymethyl)imidazolyl]azo]benzoate was measured in dimethyl sulfoxide containing 5% (v/v) water. Efficient catalys

Symmetrically Trisubstituted Triptycenes

A simple synthesis of 1,8,13- and 1,8,16-trisubstituted triptycenes is described.Diels-Alder reaction of 1,8-disubstituted anthracenes with ortho-substituted benzynes gave 15 new triptycene compounds as mixtures of the syn (1,8,13) and anti (1,8,16) trisu