103259-06-9

Basic information

• Product Name: 2-AMINO-6-METHOXYCARBONYL BENZOIC ACID
• Synonyms: 2-AMINO-6-METHOXYCARBONYL BENZOIC ACID
• CAS NO: 103259-06-9
• Molecular Formula: C₉H₉NO₄
• Molecular Weight: 195.17206
• Mol File: 103259-06-9.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 394.8±32.0 °C(Predicted)
• Appearance: /
• Density: 1.373±0.06 g/cm3(Predicted)
• Storage Temp.: 2-8°C
• PKA: 4.06±0.10(Predicted)
• CAS DataBase Reference: 2-AMINO-6-METHOXYCARBONYL BENZOIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 2-AMINO-6-METHOXYCARBONYL BENZOIC ACID(103259-06-9)
• EPA Substance Registry System: 2-AMINO-6-METHOXYCARBONYL BENZOIC ACID(103259-06-9)

Safety Data

• Hazardous Substances Data: 103259-06-9(Hazardous Substances Data)

Usage

General Description

2-Amino-6-methoxycarbonyl benzoic acid is a chemical compound known for its potential use in various chemical reactions due to its different functional groups. The compound contains an amino group, a methoxycarbonyl group, and a carboxylic acid group, contributing to its reactivity and versatility. Its precise structure allows for specific interactions and transformations. Despite the potential applicability in synthesis and chemical industry, its detailed properties and safety measures should be considered, as with any other chemical substance. Detailed information about this chemical, including its physical and chemical properties, stability, and reactivity, as well as its potential health hazards, is provided in Material Safety Data Sheets (MSDS).

Upstream product

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

Downstream Products

• 141344-48-1 methyl 2-carboxy-3-<<2-(4-carboxymethyl)imidazolyl>azo>benzoate 
• 99-05-8 meta-aminobenzoic acid 
• 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 
• 103259-26-3 N,N',N''-tris(4-hydroxyphenyl)-1,8,13-triptycenetricarboxamide 
• 103259-25-2 N,N',N''-tris(4-methylphenyl)-1,8,16-triptycenetricarboxamide 
• 136131-56-1 2-benzyl-8-carbomethoxy-1-naphthol 
• 136131-61-8 2-benzyl-5-carbomethoxy-1-naphthol 

Relevant articles and documents

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.

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

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