76746-30-0

Basic information

• Product Name: 2-Nitro-3,5-dimethoxybenzoate de methyle
• Synonyms: 2-Nitro-3,5-dimethoxybenzoate de methyle
• CAS NO: 76746-30-0
• Molecular Weight: 241.2
• Mol File: 76746-30-0.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 2-Nitro-3,5-dimethoxybenzoate de methyle(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Nitro-3,5-dimethoxybenzoate de methyle(76746-30-0)
• EPA Substance Registry System: 2-Nitro-3,5-dimethoxybenzoate de methyle(76746-30-0)

Safety Data

• Hazardous Substances Data: 76746-30-0(Hazardous Substances Data)

Upstream product

• 67-56-1 methanol 
• 113884-71-2 Acide 2-nitro-3,5-dimethoxybenzoique 
• 1132-21-4 3,5-dimethoxybenzoic acid 
• 2150-37-0 methyl 3,5-dimethoxybenzoate 

Downstream Products

• 1643324-01-9 methyl 7-methoxy-3-oxo-2-phenyl-3,4-dihydro-2H-benzo[b][1,4]oxazine-5-carboxylate 
• 105897-30-1 7-methoxy-2-methylene-3-oxo-3,4-dihydro-2H-benzo[b][1,4]oxazine-5-carboxylic acid 
• 51903-93-6 methyl 2-chloro-3,5-dimethoxybenzoate 
• 1134-08-3 2-chloro-3,5-dimethoxybenzoic acid 
• 131653-13-9 5-(3,5-Dimethoxy-2-nitro-benzyl)-6-methyl-7,8-dihydro-[1,3]dioxolo[4,5-g]isoquinolin-6-ium; iodide 
• 131653-16-2 5-(3,5-Dimethoxy-2-nitro-benzyl)-6-methyl-5,6,7,8-tetrahydro-[1,3]dioxolo[4,5-g]isoquinoline 
• 126893-22-9 1-(2-nitro-3,5-dimethoxy-benzyl)-6,7-methylenedioxy-3,4-dihydroisoquinoline 
• 131653-14-0 5-[1-(3,5-Dimethoxy-2-nitro-phenyl)-meth-(Z)-ylidene]-6-methyl-5,6,7,8-tetrahydro-[1,3]dioxolo[4,5-g]isoquinoline 

Relevant articles and documents

TERTIARY AMIDES AND METHOD OF USE

Compunds of Formula (I) and pharmaceutically acceptable salts thereof, wherein G1, G2, G3, L1, L2, and L3 are as defined in the specification, are useful in treating conditions or disorders prevented by or ameliorated by the modulation of lysophosphatidic acid receptor 1. Methods for making the compounds are described. Also described are pharmaceutical compositions of compounds of formula (I), and methods for using such compounds and compositions.

A concise synthesis of enantiopure circumdatins E, H and J

A concise total synthesis of enantiopure circumdatins E, H and J has been developed using a reductive cyclization of chiral N-prolinoyl-2-nitrobenzamides to construct the core quinazolinone ring.

Synthesis of the degradation product of auromomycin chromophore and DNA-cleaving activities of its derivatives

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