1239028-02-4

Basic information

• Product Name: methyl 5-azido-2-hydroxybenzoate
• Synonyms: methyl 5-azido-2-hydroxybenzoate
• CAS NO: 1239028-02-4
• Molecular Weight: 193.162
• Mol File: 1239028-02-4.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: methyl 5-azido-2-hydroxybenzoate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 5-azido-2-hydroxybenzoate(1239028-02-4)
• EPA Substance Registry System: methyl 5-azido-2-hydroxybenzoate(1239028-02-4)

Safety Data

• Hazardous Substances Data: 1239028-02-4(Hazardous Substances Data)

Upstream product

• 42753-75-3 methyl 5-amino-2-hydroxybenzoate 
• 89-57-6 5-Aminosalicylic Acid 

Downstream Products

• 1239028-22-8 methyl 2-hydroxy-5-[4-(2,5-dihydroxyphenyl)-1H-1,2,3-triazol-1-yl]benzoate 
• 1239028-25-1 methyl 2-hydroxy-5-[4-(2-methoxyphenyl)-1H-1,2,3-triazol-1-yl]benzoate 
• 1239028-23-9 methyl 2-hydroxy-5-[4-(3-hydroxyphenyl)-1H-1,2,3-triazol-1-yl]benzoate 
• 1239028-06-8 methyl 2-hydroxy-5-[4-(2,5-dimethoxyphenyl)-1H-1,2,3-triazol-1-yl]benzoate 
• 1239028-26-2 methyl 2-hydroxy-5-[4-(3,5-dimethoxyphenyl)-1H-1,2,3-triazol-1-yl]benzoate 
• 1239028-24-0 methyl 2-hydroxy-5-[4-(4-methoxyphenyl)-1H-1,2,3-triazol-1-yl]benzoate 
• 1290070-71-1 (5-azido-2-hydroxyphenyl)-1-piperidinylmethanone 
• 1290070-70-0 5-azido-2-hydroxy-N-propylbenzamide 
• 1290070-73-3 2-hydroxy-5-(4-phenyl-1H-1,2,3-triazol-1-yl)-N-propylbenzamide 
• 1290070-74-4 2-hydroxy-5-[4-(3-methylbutyl)-1H-1,2,3-triazol-1-yl]-N-propyl-benzamide 
• 1290070-75-5 5-(4-hexyl-1H-1,2,3-triazol-1-yl)-2-hydroxy-N-propylbenzamide 
• 1290070-76-6 5-[4-(3-chlorophenyl)-1H-1,2,3-triazol-1-yl]-2-hydroxy-N-propyl-benzamide 
• 1290070-77-7 5-[4-(3,5-difluorophenyl)-1H-1,2,3-triazol-1-yl]-2-hydroxy-N-propyl-benzamide 
• 1290070-78-8 2-hydroxy-5-[4-(4-pentylphenyl)-1H-1,2,3-triazol-1-yl]-N-propyl-benzamide 

Relevant articles and documents

Syntheses of 1,2,3-triazolyl salicylamides with inhibitory activity on lipopolysaccharide-induced nitric oxide production

A 28-membered 1,2,3-triazolyl salicylamide library was synthesized via a Cu(I)-catalyzed azide-alkyne 1,3-dipolar cycloaddition and evaluated for their abilities to inhibit NO production in LPS-activated RAW264.7 macrophage cells. Among 28 analogues, 29g showed a significant inhibitory activity (IC 50 = 12.8 μM). The inhibitory effects of 29g on LPS-mediated NO production in macrophage cells appeared to be associated with the suppression of iNOS expression.