72517-26-1

Basic information

• Product Name: Benzoic acid, 2,3-dimethoxy-6-nitro-
• CAS NO: 72517-26-1
• Molecular Formula: C9H9NO6
• Molecular Weight: 227.174
• Mol File: 72517-26-1.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: Benzoic acid, 2,3-dimethoxy-6-nitro-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid, 2,3-dimethoxy-6-nitro-(72517-26-1)
• EPA Substance Registry System: Benzoic acid, 2,3-dimethoxy-6-nitro-(72517-26-1)

Safety Data

• Hazardous Substances Data: 72517-26-1(Hazardous Substances Data)

Upstream product

• 86-51-1 2,3-dimethyoxybenzaldehyde 
• 2531-63-7 5,6-dimethoxy-2-nitrobenzaldehyde 
• 7440-44-0 pyrographite 
• 860749-16-2 2,3-dimethoxy-4,6-dinitro-toluene 
• 860573-21-3 2,3-dimethoxy-4-methyl-5-nitro-aniline 
• 111042-36-5 2-Hydroxy-3-methoxy-6-nitrobenzaldehyde, sodium salt 
• 148-53-8 3-methoxy-2-hydroxybenzaldehyde 
• 2426-60-0 2-Hydroxy-3-methoxy-6-nitrobenzaldehyde benzenesulfonate 
• 2426-85-9 2-Hydroxy-3-methoxybenzaldehyde benzenesulfonate 
• 845513-40-8 2-(2,3-dimethoxy-6-nitro-phenyl)-5-oxo-tetrahydro-furan-3-carboxylic acid 
• 82209-17-4 1,2-dimethyoxy-3-methyl-4-nitrobenzene 
• 518-90-1 3,4-dimethoxy-phthalic acid 

Downstream Products

• 103580-03-6 Ethyl 2,3-dimethoxy-6-nitrobenzoate 
• 68452-40-4 (2,3-dimethoxy-6-nitro-phenyl)-acetic acid 
• 60241-74-9 2,3,6-trimethoxybenzoic acid 
• 81595-28-0 2-(dimethylamino)-5,6-dihydroxy-3,4-dihydroquinazoline hydrobromide 
• 106107-49-7 ethyl 2-carboxy-3,4-dimethoxybenzenecarbamate 
• 81595-20-2 2-(dimethylamino)-5,6-dimethoxy-4(1H)-quinazolinone 
• 72517-27-2 2,3-dimethoxy-5,6-dinitro-benzoic acid 
• 98263-19-5 2,3-dimethoxy-6-nitrobenzoyl chloride 
• 709-09-1 3,4-dimethoxynitrobenzene 
• 636-93-1 5-nitroguaiacol 
• 5653-53-2 6-hydroxy-2,3-dimethoxy-benzoic acid 
• 5653-51-0 6-amino-2,3-dimethoxybenzoic acid 
• 99055-59-1 methyl 2-nitro-5,6-dimethoxybenzoate 
• 99069-16-6 (2,3-dimethoxy-6-nitro-phenyl)-acetic acid amide 

Relevant articles and documents

NEW DS DNA BINDING FLUORESCENT DYES

The present invention is directed to a fluorescent dye comprising a benzothiazolium moiety and a pyrimidinium moiety connected by a mono-methine bridge, characterized in that (i) the 2-position of the pyrimidine carries a substituent which starts with a C

Process for preparing 5,6-dialkoxy-4-alkyl-2(1H)-quinazolinones

A method for preparing 5,6-dialkoxy-4-alkyl-quinazolinones is described. The 5,6-dialkoxy-4-alkyl-quinazolinones are active cardiotonic agents.

Substituted 5,6-dialkoxyquinazoline derivatives

Quinazoline derivatives having an oxy substituent in 5 and 6 positions are described. The novel quinazoline derivatives are useful as cardiotonic agents.