6945-76-2

Basic information

• Product Name: 1,4-dimethoxy-2,3-dinitrobenzene
• Synonyms: benzene, 1,4-dimethoxy-2,3-dinitro-
• CAS NO: 6945-76-2
• Molecular Formula: C₈H₈N₂O₆
• Molecular Weight: 228.1589
• Mol File: 6945-76-2.mol
• Article Data: 31

Chemical Properties

• Boiling Point: 410.4°C at 760 mmHg
• Flash Point: 205.7°C
• Density: 1.416g/cm³
• Vapor Pressure: 1.43E-06mmHg at 25°C
• Refractive Index: 1.567
• CAS DataBase Reference: 1,4-dimethoxy-2,3-dinitrobenzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1,4-dimethoxy-2,3-dinitrobenzene(6945-76-2)
• EPA Substance Registry System: 1,4-dimethoxy-2,3-dinitrobenzene(6945-76-2)

Safety Data

• Hazardous Substances Data: 6945-76-2(Hazardous Substances Data)

Usage

Appearance

Yellow crystalline solid

Uses

a. Synthesis of dyes
b. Synthesis of pharmaceuticals
c. Synthesis of other organic compounds

Application

Test reagent for detection and quantification of amino acids and amines

Upstream product

• 150-78-7 1,4-dimethoxybezene 

Downstream Products

• 120644-07-7 1-(3,6-dimethoxy-2-nitrophenyl)pyrrolidine 
• 120644-08-8 1-(3,6-dimethoxy-2-nitrophenyl)piperidine 
• 7767-55-7 2,3-Diamino-1,4-dimethoxybenzene dihydrochloride 
• 1260530-38-8 10,13-dimethoxy-11,12-bis(p-toluenesulfamido)-dipyrido[3,2-a:2',3'-c]phenazine 
• 1260530-30-0 3,6-dimethoxybenzene-4,5-bis(p-toluenesulfonamido)benzene 
• 120644-09-9 4-(3,6-dimethoxy-2-nitrophenyl)morpholine 
• 101281-19-0 bis-(3,6-dimethoxy-2-nitro-phenyl)-sulfide 
• 40328-95-8 2,3-diamino-1,4-dimethoxybenzene 
• 89427-14-5 4,7-dimethoxy-2-trifluoromethyl-benzimidazole 

Relevant articles and documents

Anthrathiadiazole Derivatives: Synthesis, Physical Properties and Two-photon Absorption

Anthrathiadiazole is a key synthon for the construction of large azaacenes, however, the attachment of different substituents onto the skeleton of anthrathiadiazole is difficult but highly desirable because it could be easy to enrich the structures of aza

Identification of ortho-naphthoquinones as anti-AML agents by highly efficient oxidation of phenols

A straightforward method for synthesizing ortho-naphthoquinones was identified using an easily available cobalt–Schiff base complex. Efficient oxidation of phenols to ortho-naphthoquinones was useful in obtaining compounds with potent biological activity

Light-actuated resorcin[4]arene cavitands

A light-actuated resorcin[4]arene cavitand equipped with two quinone (Q) and two opposite Ru(II)-based photosensitizing walls was synthesized and investigated. The cavitand is capable of switching from an open to a contracted conformation upon reduction of the two Q to the corresponding SQ radical anions by intramolecular photoinduced electron transfer in the presence of a sacrificial donor. The molecular switch was investigated by cyclic and rotating disc voltammetry, UV–Vis–NIR spectroelectrochemistry, transient absorption, NMR, and EPR spectroscopy. This study provides the basis for the development of future light-activated switches and molecular actuating nanodevices.