116324-66-4

Basic information

• Product Name: METHYL 2-AMINO-3,6-DIMETHOXYBENZOATE
• Synonyms: METHYL 2-AMINO-3,6-DIMETHOXYBENZOATE;3,6-diMethoxy-2-Methylbenzoic acid
• CAS NO: 116324-66-4
• Molecular Formula: C₁₀H₁₂O₄
• Molecular Weight: 196.2
• Mol File: 116324-66-4.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 344.1°C at 760 mmHg
• Flash Point: 167.1°C
• Appearance: /
• Density: 1.189g/cm³
• Vapor Pressure: 6.72E-05mmHg at 25°C
• Refractive Index: 1.538
• PKA: 3.62±0.31(Predicted)
• CAS DataBase Reference: METHYL 2-AMINO-3,6-DIMETHOXYBENZOATE(CAS DataBase Reference)
• NIST Chemistry Reference: METHYL 2-AMINO-3,6-DIMETHOXYBENZOATE(116324-66-4)
• EPA Substance Registry System: METHYL 2-AMINO-3,6-DIMETHOXYBENZOATE(116324-66-4)

Safety Data

• Hazardous Substances Data: 116324-66-4(Hazardous Substances Data)

Usage

InChI:InChI=1/C10H13NO4/c1-13-6-4-5-7(14-2)9(11)8(6)10(12)15-3/h4-5H,11H2,1-3H3

Upstream product

• 93-02-7 2,5-dimethoxybenzaldehyde 
• 2785-98-0 2,5-dimethoxybenzoic acid 
• 74-88-4 methyl iodide 
• 121625-00-1 3,6-dimethoxyl-2-methylbenzaldehyde 
• 567-61-3 2-hydroxy-6-methylbenzoic acid 
• 5981-42-0 3,6-dihydroxy-2-methyl-benzoic acid 
• 77-78-1 dimethyl sulfate 

Downstream Products

• 14597-12-7 3,6-dimethoxyphthalic anhydride 
• 177036-31-6 4,7-dihydroxyisobenzofuran-1(3H)-one 
• 116324-51-7 3,6-dimethoxy-2-methylbenzoic acid chloride 
• 1260694-74-3 C₁₆H₁₅BrO₄ 
• 1260694-70-9 phenyl 3,6-dimethoxy-2-methylbenzoate 
• 1260694-68-5 C₂₂H₂₀O₅S 
• 1260694-76-5 C₂₂H₂₀O₄S 
• 1268463-50-8 phenyl 6-hydroxy-3-methoxy-2-methylbenzoate 
• 1268463-51-9 phenyl 6-(tert-butoxycarbonyloxy)-3-methoxy-2-methylbenzoate 
• 1268463-54-2 phenyl 6-(benzyloxy)-3-methoxy-2-methylbenzoate 
• 1268463-55-3 phenyl 2-(benzyloxy)-5-methoxy-6-methyl-3-nitrobenzoate 
• 1268463-56-4 phenyl 2-(benzyloxy)-5-methoxy-6-methyl-3-aminobenzoate 
• 1268463-57-5 phenyl 2-(benzyloxy)-3-(bis(tert-butoxycarbonyl)amino)-5-methoxy-6-methylbenzoate 
• 1268463-74-6 phenyl 2-(benzyloxy)-3-bromo-5-methoxy-6-methylbenzoate 

Relevant articles and documents

Total Synthesis of (+)-Nivetetracyclate A

A stereoselective synthetic approach to the natural product (+)-nivetetracyclate A is reported. The tetracyclic skeleton was assembled in a convergent manner by an alkylation to a diarylmethane and subsequent Friedel-Crafts acylation. Further key steps ar

TETRACYCLINE COMPOUNDS

The present invention is directed to a compound represented by Structural Formula (1): or a pharmaceutically acceptable salt thereof. The variables for Structural Formula (I) are defined herein. Also described is a pharmaceutical composition comprising th