1770-37-2

Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule of the compound.

Explanation

This is an alternative name for the compound, which is derived from its structure and functional groups.

Explanation

The chemical structure describes the arrangement of atoms and bonds in the molecule.

Explanation

Functional groups are specific groups of atoms within a molecule that have characteristic chemical properties and reactivity.

Explanation

The compound serves as a starting material or building block for the production of other chemicals and may be added to various products to enhance their properties.

Explanation

Due to potential harmful effects, it is essential to take appropriate safety measures when working with this chemical, such as using personal protective equipment and working in a well-ventilated area.

Explanation

The compound could pose health risks or environmental concerns if it is not handled, stored, or disposed of correctly.

Chemical structure

Aromatic ring with two amine groups (-NH2) at the 1,2 positions and two butoxy groups (-OBu) at the 4,5 positions.

Functional groups

Aromatic ring, amine groups, and butoxy groups.

Use

Intermediate in the synthesis of organic compounds and potential additive in industrial and consumer products.

Safety precautions

Handle with caution and follow safety guidelines.

Potential hazards

May have harmful effects if not properly managed.

Upstream product

• 120-80-9 benzene-1,2-diol 
• 101270-47-7 acetic acid-(4,5-dibutoxy-2-nitro-anilide) 
• 20367-37-7 1,2-dibutoxy-4,5-dinitrobenzene 

Relevant academic research and scientific papers

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

A NOVEL QUINOXALINE COMPOUND FOR ULTRAVIOLET ABSORBERS

PURPOSE: A novel quinoxaline compound, isomer thereof, precursor drug thereof, or pharmaceutically acceptable salt thereof is provided to absorb UVA and UVB. CONSTITUTION: A quinoxaline compound is denoted by chemical formula 1. An UV absorber or pharmaceutical or cosmetic composition for antiaging contains the quinoxaline compound, isomer thereof, precursor drug thereof, or pharmaceutically acceptable salt, hydrate, or solvate thereof as an active ingredient.

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

Rapid synthesis of new discotic liquid crystals based on diquinoxalino[2,3-a:2′,3′-c]phenazine containing hexakis(alkoxy) side arms

The condensation of 1,2-bisalkoxy-4,5-diaminobenzene 2a-e derivatives with freshly prepared hexaketocyclohexane give hexakis(alkoxy)diquinoxalino[2,3-a:2′,3′-c]phenazines in good yield. DSC and polarization microscopy showed HATOC6 has both the crystalline (K) to mesophase (M) and the mesophase (M) to isotropic (I) phase transitions. Importantly, the alkoxy substituted compound synthesized showed an M-I transition because of greater stability, whereas the reported alkyl-thiol decomposes after the mesophase.

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.