695816-73-0

Basic information

• Product Name: 1,2-bis(hexyloxy)-4,5-dinitrobenzene
• Synonyms: 1,2-bis(hexyloxy)-4,5-dinitrobenzene
• CAS NO: 695816-73-0
• Molecular Formula: C₁₈H₂₈N₂O₆
• Molecular Weight: 368.42472
• Mol File: 695816-73-0.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1,2-bis(hexyloxy)-4,5-dinitrobenzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-bis(hexyloxy)-4,5-dinitrobenzene(695816-73-0)
• EPA Substance Registry System: 1,2-bis(hexyloxy)-4,5-dinitrobenzene(695816-73-0)

Safety Data

• Hazardous Substances Data: 695816-73-0(Hazardous Substances Data)

Usage

Appearance

Yellow crystalline solid

Usage

High energy density material for propellants and explosives

Nitro content

High, contributing to its explosive properties

Additional use

Sensitizer in explosives to increase sensitivity to initiation

Hazard classification

Classified as a hazardous material

Safety precautions

Causes irritation to eyes, skin, and respiratory system upon exposure; handle with caution

Upstream product

• 77400-30-7 1,2-dihydroxy-4,5-dinitrobenzene 
• 638-45-9 1-Iodohexane 
• 120-80-9 benzene-1,2-diol 
• 111-25-1 1-bromo-hexane 
• 94259-20-8 1,2-dihexyloxybenzene 

Downstream Products

• 1190978-94-9 4,7-dibromo-5,6-bis(hexyloxy)benzo[c][1,2,5]thiadiazole 
• 86723-21-9 1,2-bis(hexyloxy)-4,5-diaminobenzene 

Relevant articles and documents

Dynamic Polymer Free Volume Monitored by Single-Molecule Spectroscopy of a Dual Fluorescent Flapping Dopant

Single-molecule spectroscopy (SMS) of a dual fluorescent flapping molecular probe (N-FLAP) enabled real-time nanoscale monitoring of local free volume dynamics in polystyrenes. The SMS study was realized by structural improvement of a previously reported

High-performance dye-sensitized solar cells based on 5,6-bis-hexyloxy- benzo[2,1,3]thiadiazole

New dipolar compounds containing a 5,6-bis-hexyloxy-benzo[2,1,3]thiadiazole entity in the conjugated spacer between the electron donating arylamine and the electron accepting 2-cyanoacrylic acid have been synthesized. These compounds were used as the sensitizers for efficient dye-sensitized solar cells. Compared to the congeners without the hexyloxy chains, the new dyes effectively suppress the dark currents and significantly improve the cell performance. The best conversion efficiency reached ～92% of the N719-based standard DSSC fabricated and measured under similar conditions (AM 1.5 irradiation). The Royal Society of Chemistry 2012.

In Situ Synthesis of Hexakis(alkoxy)diquinoxalino[2,3-a:2′,3′ -c]phenazines: Mesogenic Phase Transition of the Electron-Deficient Discotic Compounds

2,3,8,9,14,15-Hexakis(alkoxy)diquinoxalino[2,3-a:2′,3′- c]phenazines with alkyl side chains varying from 6 to 12 carbon atoms were readily synthesized by the condensation of hexaketocyclohexane with the respective 1,2-bisalkoxy-4,5-diaminobenzene. Polariz