15866-67-8

Basic information

• Product Name: 1-nitro-4-(4-phenylbuta-1,3-dien-1-yl)benzene
• CAS NO: 15866-67-8
• Molecular Formula: C₁₆H₁₃NO₂
• Molecular Weight: 251.2799
• Mol File: 15866-67-8.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 418.3°C at 760 mmHg
• Flash Point: 196.3°C
• Density: 1.19g/cm³
• Vapor Pressure: 8.04E-07mmHg at 25°C
• Refractive Index: 1.677
• CAS DataBase Reference: 1-nitro-4-(4-phenylbuta-1,3-dien-1-yl)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-nitro-4-(4-phenylbuta-1,3-dien-1-yl)benzene(15866-67-8)
• EPA Substance Registry System: 1-nitro-4-(4-phenylbuta-1,3-dien-1-yl)benzene(15866-67-8)

Safety Data

• Hazardous Substances Data: 15866-67-8(Hazardous Substances Data)

Usage

Appearance

Yellow crystalline

Type of compound

Nitro-substituted aromatic compound

Uses

Precursor in the synthesis of various organic molecules and polymers, production of dyes, pigments, and pharmaceuticals

Reactivity

Can undergo reduction, nitration, and alkylation reactions

Toxicity

Low acute toxicity but may pose health risks if inhaled or ingested in large quantities

Safety precautions

Handle and store with proper safety measures to prevent accidental exposure.

Upstream product

• 555-16-8 4-nitrobenzaldehdye 
• 1530-35-4 cinnamyltriphenylphosphonium chloride 
• 2767-70-6 (p-nitrobenzyl)triphenylphosphonium bromide 
• 104-55-2 3-phenyl-propenal 
• 16939-57-4 (E)-buta-1,3-dienylbenzene 
• 586-78-7 para-nitrophenyl bromide 
• 39980-20-6 dimethyl (4-nitrobenzyl)phosphonate 
• 2609-49-6 diethyl p-nitrobenzylphosphonate 
• 100-11-8 1-bromomethyl-4-nitro-benzene 

Downstream Products

• 1170321-09-1 1-(4-nitrophenyl)-4-phenylnaphthalene 

Relevant articles and documents

Influence of imidazolium ionic liquids on fluorescence of push-pull diphenylbutadienes

A series of donor-acceptor substituted diphenylbutadienes have been synthesized and their fluorescence properties in organic solvents and imidazolium ionic liquid media were investigated. Substituted diphenylbutadienes show remarkable solvatochromic emiss

Electrochemical reduction of certain fluorenyl and xanthenyl olefins

The reduction of certain fluorene and xanthene containing olefins at a mercury electrode using cyclic voltammetry has been investigated.In DMF, fluorene-9-(4-nitrophenyl)methylene (1) reveals two distinct reversible one-electron redox waves corresponding to anion radical and dianion formation.Some other olefins particularly stilbenes (9-14) and substituted propenones (7,8) show commonality in the emergence of at least one distinct reversible reduction couple.Anion radicals of nearly all of the olefins (1-14) studied in this work generated electrochemically or by chemical 1-electron reductants, exhibited considerable stability.

Irreversible enzyme inhibitors. LXXXVI. Hydrophobic bonding to dihydrofolic reductase. 8. Substituted-1-aryl-4,6-diamino-1,2-dihydro-2,2-dimethyl-s-triazines.

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