50413-30-4

Basic information

• Product Name: 2-AMINO-4-METHOXY-BENZOIC ACID METHYL ESTER
• Synonyms: METHYL 2-AMINO-4-METHOXYBENZOATE;2-AMINO-4-METHOXY-BENZOIC ACID METHYL ESTER;methyl2-amino-4-methoxylbenzoate
• CAS NO: 50413-30-4
• Molecular Formula: C₉H₁₁NO₃
• Molecular Weight: 181.19
• Mol File: 50413-30-4.mol
• Article Data: 17

Chemical Properties

• Melting Point: 116-118 °C
• Boiling Point: 313.7 °C at 760 mmHg
• Flash Point: 158.8 °C
• Appearance: /
• Density: 1.179 g/cm³
• Vapor Pressure: 0.000488mmHg at 25°C
• Refractive Index: 1.55
• Storage Temp.: Keep in dark place,Sealed in dry,Room Temperature
• PKA: 2.17±0.10(Predicted)
• CAS DataBase Reference: 2-AMINO-4-METHOXY-BENZOIC ACID METHYL ESTER(CAS DataBase Reference)
• NIST Chemistry Reference: 2-AMINO-4-METHOXY-BENZOIC ACID METHYL ESTER(50413-30-4)
• EPA Substance Registry System: 2-AMINO-4-METHOXY-BENZOIC ACID METHYL ESTER(50413-30-4)

Safety Data

• Hazardous Substances Data: 50413-30-4(Hazardous Substances Data)

Usage

General Description

2-Amino-4-methoxy-benzoic acid methyl ester, also known as anthranilic acid, is a chemical compound with the molecular formula C9H9NO3. It is an organic compound that is commonly used as a precursor in the synthesis of pharmaceuticals and dyes. It is a white solid with a faint odor and is soluble in organic solvents. It is a versatile compound with various industrial applications, including as a building block in the production of drugs, agrochemicals, and other chemicals. It is important to handle this chemical with care and follow proper safety protocols due to its potential hazardous properties.

InChI:InChI=1/C9H11NO3/c1-12-6-3-4-7(8(10)5-6)9(11)13-2/h3-5H,10H2,1-2H3

Upstream product

• 67-56-1 methanol 
• 4294-95-5 4-methoxyanthranilic acid 
• 52351-75-4 6-methoxyisatin 
• 6966-87-6 2-(hydroxyimino)-N-(3-methoxyphenyl)acetamide 
• 536-90-3 m-Anisidine 
• 181871-73-8 methyl 4-methoxy-2-nitrobenzoate 
• 33844-21-2 2-nitro-4-methoxybenzoic acid 
• 121-98-2 methyl 4-methoxybenzoate 
• 75-18-3 dimethylsulfide 
• 201230-82-2 carbon monoxide 
• 153898-63-6 2-iodo-5-methoxyaniline 

Downstream Products

• 108489-18-5 N-(5-methoxy-2-methoxycarbonyl-phenyl)-succinamic acid 
• 16064-24-7 7-methoxyquinazoline-4(3H)-one 
• 100038-83-3 N-<5-methoxy-2-(methoxycarbonyl)phenyl>anthranilic acid 
• 93009-62-2 methyl 4-methoxy-2-((4-methylphenyl)sulfonamido)benzoate 
• 71083-64-2 1,4-dihydro-7-methoxy-4-oxo-quinoline-3-carbonitrile 
• 73387-74-3 4-chloro-7-methoxy-quinoline-3-carbonitrile 
• 187601-84-9 8-methoxy-1,2,3,4-tetrahydro-5H-benzo[b]azepin-5-one 
• 187601-82-7 8-methoxy-1-tosyl-1,2,3,4-tetrahydro-5H-benzo[b]azepin-5-one 
• 200010-59-9 8-Methoxy-1-(toluene-4-sulfonyl)-2,3-dihydro-1H-benzo[b]azepine-4,5-dione 4-oxime 
• 200010-60-2 8-Methoxy-1-(toluene-4-sulfonyl)-2,3-dihydro-1H-benzo[b]azepine-4,5-dione 4-(O-methyl-oxime) 
• 200010-64-6 N-[8-Methoxy-5-oxo-1-(toluene-4-sulfonyl)-2,3,4,5-tetrahydro-1H-benzo[b]azepin-4-yl]-acetamide 
• 200010-58-8 ethyl 8-methoxy-5-oxo-1-tosyl-2,3,4,5-tetrahydro-1H-benzo[b]azepine-4-carboxylate 
• 200010-72-6 N-[8-Methoxy-5-oxo-1-(toluene-4-sulfonyl)-2,3,4,5-tetrahydro-1H-benzo[b]azepin-4-yl]-propionamide 
• 200010-62-4 3-[5-Hydroxy-8-methoxy-4-[(E)-methoxyimino]-1-(toluene-4-sulfonyl)-2,3,4,5-tetrahydro-1H-benzo[b]azepin-5-yl]-propionic acid ethyl ester 

Relevant articles and documents

Tunable Electrosynthesis of Anthranilic Acid Derivatives via a C-C Bond Cleavage of Isatins

A facile and direct electrocatalytic C-C bond cleavage/functionalization reaction of isatins was developed. With isatins as the amino-attached C1 sources, a variety of aminobenzoates, and aminobenzamides were synthesized in moderate to good yields under mild conditions.

Antituberculosis Activity of the Antimalaria Cytochrome bcc Oxidase Inhibitor SCR0911

The ability to respire and generate adenosine triphosphate (ATP) is essential for the physiology, persistence, and pathogenicity of Mycobacterium tuberculosis, which causes tuberculosis. By employing a lead repurposing strategy, the malarial cytochrome bc

HETEROCYCLIC ACYL HYDRAZONE LINKERS, METHODS AND USES THEREOF

The present application is directed to compounds of Formula (I): compounds of Formula (II): compounds of Formula (III): and compounds of Formula (IV): compositions comprising these compounds and their uses, for example as medicaments and /or diagnostics.