37592-20-4

Basic information

• Product Name: 1,4-diprop-2-enoxybenzene
• Synonyms: 1,4-diprop-2-enoxybenzene
• CAS NO: 37592-20-4
• Molecular Formula: C₁₂H₁₄O₂
• Molecular Weight: 190.24
• Mol File: 37592-20-4.mol
• Article Data: 29

Chemical Properties

• Boiling Point: 284.7°Cat760mmHg
• Flash Point: 109.3°C
• Appearance: /
• Density: 0.982g/cm³
• Vapor Pressure: 0.00502mmHg at 25°C
• Refractive Index: 1.506
• CAS DataBase Reference: 1,4-diprop-2-enoxybenzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1,4-diprop-2-enoxybenzene(37592-20-4)
• EPA Substance Registry System: 1,4-diprop-2-enoxybenzene(37592-20-4)

Safety Data

• Hazardous Substances Data: 37592-20-4(Hazardous Substances Data)

Usage

Physical state

Clear, colorless liquid

Odor

Strong

Uses

a. Production of polymers
b. Flavoring agent in the food industry
c. Manufacturing of resins
d. Precursor to other organic compounds
e. Solvent in various industrial processes

Environmental impact

Toxic to aquatic organisms, harmful effects on the environment if not properly managed

Health risks

Prolonged exposure can cause irritation to the eyes, skin, and respiratory system

Precautions

Handle with care due to potential environmental and health risks

InChI:InChI=1/C12H14O2/c1-3-9-13-11-5-7-12(8-6-11)14-10-4-2/h3-8H,1-2,9-10H2

Upstream product

• 106-95-6 allyl bromide 
• 123-31-9 hydroquinone 
• 35466-83-2 allyl methyl carbonate 
• 591-87-7 Allyl acetate 
• 107-05-1 3-chloroprop-1-ene 

Downstream Products

• 52210-93-2 2-((4-(allyloxy)phenoxy)methyl)oxirane 
• 2425-01-6 1,4-bis(oxiran-2-ylmethoxy)benzene 
• 7734-54-5 3,3'-(1,4-phenylenebis(oxy))bis(propane-1,2-diol) 
• 123-31-9 hydroquinone 
• 2444-19-1 4-hydroxyphenyl benzoate 
• 103-16-2 4-Benzyloxyphenol 
• 6411-34-3 4-allyloxyphenol 
• 664324-38-3 2-allyl-4-(allyloxy)phenol 
• 24535-81-7 1,4-Phenylen-bis-oxyacetaldehyd 
• 3732-21-6 11-Brom-undecansaeure-(4-nitro-2,5-diallyloxy-anilid) 
• 3732-20-5 11-Brom-undecansaeure-(2,5-diallyloxy-anilid) 
• 3953-43-3 1,4-Bis-(11-brom-undecanoyl-amino)-2,5-diallyloxy-benzol 
• 911381-40-3 1,4-diacetoxy-2,5-diallyl-benzene 

Relevant articles and documents

Spreading of benquitrione droplets on superhydrophobic leaves through pillar[5]arene-based host-guest chemistry

Spreading of agricultural sprays on plant surfaces is a significant task as it helps decrease pesticide usage and thereby reduces the risk of environmental pollution. Here, we report a method of increasing the spreading of herbicide benquitrione droplets

Design and synthesis of novel propellanes by using claisen rearrangement and ring-closing metathesis as the key steps

Novel hexacyclic caged compounds are prepared by a combination of Claisen rearrangement and ring-closing metathesis (RCM). Additionally, a Grignard reaction in conjugation with RCM produced intricate hexacyclic caged molecules.

Ring-Closing Metathesis Approach to Cage Propellanes Containing Oxepane and Tetrahydrofuran Hybrid System

The preparation of a variety of structurally interesting oxygenated cage compounds involving atom-economic processes such as Claisen rearrangement, Diels-Alder reaction, [2+2] photocycloaddition, and ring-closing metathesis (RCM) as key steps is reported.

Palladium-catalyzed anti-Markovnikov oxidative acetalization of activated olefins with iron(iii) sulphate as the reoxidant

This paper discloses the efficient palladium-catalyzed anti-Markovnikov oxidative acetalization of activated terminal olefins with iron(iii) sulfate as the reoxidant. This methodology requires mild reaction conditions and shows high regioselectivity toward anti-Markovnikov products and compatibility with a wide range of functional groups. Iron(iii) sulphate was the sole reoxidant used in this method. Various olefins like vinylarenes, aryl-allylethers, aryl or benzyl acrylates and homoallylic alcohols all reacted well providing anti-Markovnikov acetals, some of which represent orthogonally functionalized 1,3- and 1,4-dioxygenated compounds.