20367-37-7

Basic information

• Product Name: 1,2-DIBUTOXY-4,5-DINITRO-BENZENE
• Synonyms: 1,2-DIBUTOXY-4,5-DINITRO-BENZENE
• CAS NO: 20367-37-7
• Molecular Formula: C₁₄H₂₀N₂O₆
• Molecular Weight: 312.32
• Mol File: 20367-37-7.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1,2-DIBUTOXY-4,5-DINITRO-BENZENE(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-DIBUTOXY-4,5-DINITRO-BENZENE(20367-37-7)
• EPA Substance Registry System: 1,2-DIBUTOXY-4,5-DINITRO-BENZENE(20367-37-7)

Safety Data

• Hazardous Substances Data: 20367-37-7(Hazardous Substances Data)

Upstream product

• 120-80-9 benzene-1,2-diol 
• 4956-77-8 3,4-di(butyloxy)nitrobenzene 
• 7697-37-2 nitric acid 
• 20367-35-5 1,2-dibutoxybenzene 

Downstream Products

• 1770-37-2 1,2,-diamino-4,5-dibutoxybenzene 

Relevant articles and documents

Synthesis and photovoltaic characterization of triarylamine-substituted quinoxaline push–pull dyes to improve the performance of dye-sensitized solar cells

Novel unsymmetrical organic sensitizers having donor, π-spacer, and anchoring groups were designed and synthesized for dye-sensitized solar cell (DSSC) application. The dyes 3-{4-[7-(4-{bis[4-(hexyl)phenyl]amino} phenyl)-11,12-dibutoxy-1,4,5,8-tetrahydrod

Azolium-linked cyclophanes: Effects of structure, solvent, and counteranions on solution conformation behavior

(Chemical Equation Presented) This paper describes the synthesis, structural characterization, and solution behavior of some xylyl-linked imidazolium and benzimidazolium cyclophanes decorated with alkyl or alkoxy groups. The addition of alkyl/alkoxy chain

Acetoxylation of 6,7-dialkoxy-substituted 1,4-dihydroquinoxaline-2,3-diones (QXs) using fuming nitric acid in acetic acid: A facile synthesis of 5-acyloxy-6,7-dialkoxy QXs

Treatment of 6,7-dialkoxy-1,4-dihydroquinoxaline-2,3-diones 3 with fuming nitric acid in acetic acid at 25°C resulted in an acetoxylation reaction, giving 5-acetoxy-6,7-dialkoxy-1,4-dihydroquinoxaline-2,3-diones 4 in moderate yields. A mechanism involving ipso attack of nitronium ion as the first step is proposed.