117573-59-8

Basic information

• Product Name: Benzoic acid, 2-azido-4,5-dimethoxy-
• CAS NO: 117573-59-8
• Molecular Formula: C9H9N3O4
• Molecular Weight: 223.188
• Mol File: 117573-59-8.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Benzoic acid, 2-azido-4,5-dimethoxy-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid, 2-azido-4,5-dimethoxy-(117573-59-8)
• EPA Substance Registry System: Benzoic acid, 2-azido-4,5-dimethoxy-(117573-59-8)

Safety Data

• Hazardous Substances Data: 117573-59-8(Hazardous Substances Data)

Upstream product

• 5653-40-7 2-Amino-4,5-dimethoxybenzoic acid 

Downstream Products

• 187083-38-1 (2-Azido-4,5-dimethoxy-phenyl)-((S)-2-hydroxymethyl-pyrrolidin-1-yl)-methanone 
• 1191076-60-4 C₂₂H₂₂N₄O₄ 
• 923975-46-6 C₁₄H₁₆N₄O₆ 
• 923975-36-4 C₁₄H₁₆N₄O₅ 
• 144386-09-4 5,11-Bis(2-azido-4,5-dimethoxybenzoyl)dibenzo<1,5>diazocine-6,12(5H,11H)-dione 
• 187083-45-0 (S)-1-(2-Azido-4,5-dimethoxy-benzoyl)-pyrrolidine-2-carbaldehyde 
• 428817-10-1 furan-2-carboxylic acid (2-azido-4,5-dimethoxy-benzoyl)-thiophen-2-ylmethyl-amide 
• 706816-86-6 (2S,4R)-1-(2-Azido-4,5-dimethoxy-benzoyl)-4-methanesulfonyloxy-pyrrolidine-2-carboxylic acid methyl ester 
• 706816-89-9 (2S,4S)-4-Azido-1-(2-azido-4,5-dimethoxy-benzoyl)-pyrrolidine-2-carboxylic acid methyl ester 
• 752214-34-9 (S)-1-(2-Azido-4,5-dimethoxy-benzoyl)-pyrrolidine-2-carboxylic acid methyl ester 
• 382137-66-8 (2S,4R)-1-(2-Azido-4,5-dimethoxy-benzoyl)-4-hydroxy-pyrrolidine-2-carboxylic acid methyl ester 
• 5653-40-7 2-Amino-4,5-dimethoxybenzoic acid 
• 187275-91-8 2-Azido-4,5-dimethoxybenzoyl chloride 

Relevant articles and documents

A reliable one-pot synthesis of aryl azides from aryl amines using organotin azides as effective and recoverable reagents

A mild and mass-efficient procedure based on the one-pot diazotization-azidodediazoniation of aromatic amines is described. A wide range of aryl azides are obtained in moderate to high yields by using tributyltin azide as an effective and reusable azide source in the presence of p-toluenesulfonic acid at room temperature. The method was also successfully applied employing an insoluble polymer-supported organotin azide.

Efficient conversion of aromatic amines into azides: A one-pot synthesis of triazole linkages

An efficient and improved procedure for the preparation of aromatic azides and their application in the Cu(I)-catalyzed azide-alkyne 1,3-dipolar cycloaddition ("click reaction") is described. The synthesis of aromatic azides from the corresponding amies i