24824-86-0

Basic information

• Product Name: 1-(allyloxy)-3-chlorobenzene
• Synonyms: 1-(allyloxy)-3-chlorobenzene
• CAS NO: 24824-86-0
• Molecular Weight: 168.623
• Mol File: 24824-86-0.mol
• Article Data: 13

Chemical Properties

• CAS DataBase Reference: 1-(allyloxy)-3-chlorobenzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(allyloxy)-3-chlorobenzene(24824-86-0)
• EPA Substance Registry System: 1-(allyloxy)-3-chlorobenzene(24824-86-0)

Safety Data

• Hazardous Substances Data: 24824-86-0(Hazardous Substances Data)

Usage

Physical state

Colorless liquid

Odor

Sweet, floral

Uses

a. Flavoring agent in food and beverage industry
b. Production of pharmaceuticals
c. Production of fragrances
d. Synthesis of other organic compounds

Safety precautions

a. Harmful if ingested
b. Harmful if inhaled
c. Harmful if absorbed through the skin

Environmental hazard

Yes, should be disposed of properly to minimize environmental impact

Upstream product

• 108-43-0 3-monochlorophenol 
• 106-95-6 allyl bromide 
• 420-12-2 thirane 
• 3046-27-3 sodium m-chlorophenoxide 
• 107-05-1 3-chloroprop-1-ene 
• 1072-43-1 propylene sulphide 
• 179938-92-2 (Z)-1-chloro-3-(prop-1-en-1-yloxy)benzene 

Downstream Products

• 58621-36-6 2-allyl-5-chlorophenol 
• 179938-92-2 (Z)-1-chloro-3-(prop-1-en-1-yloxy)benzene 
• 58621-48-0 6-Chlor-2-methyl-coumaran 
• 58621-35-5 2-allyl-3-chlorophenol 
• 1227416-13-8 C₂₁H₁₇ClN₄O₂ 
• 1227416-12-7 C₂₁H₁₇ClN₄O₂ 
• 37483-53-7 ethyl 4-(3-chlorophenoxy)butanoate 
• 2211-95-2 1-(3-chlorophenoxy)-2,3,epoxypropane 
• 108-43-0 3-monochlorophenol 
• 1227416-15-0 C₂₂H₁₉ClN₄O₂ 
• 1227416-14-9 C₂₂H₁₉ClN₄O₂ 
• 1227418-30-5 C₁₀H₁₁ClO 
• 1227418-29-2 C₁₀H₁₁ClO 
• 117690-93-4 4-(4-cyanobutoxy)-2-chloro-5-propylacetophenone 

Relevant articles and documents

Nickel-catalyzed deallylation of aryl allyl ethers with hydrosilanes

An efficient and mild catalytic deallylation method of aryl allyl ethers is developed, with commercially available Ni(COD)2 as catalyst precursor, simple substituted bipyridine as ligand and air-stable hydrosilanes. The process is compatible with a variety of functional groups and the desired phenol products can be obtained with excellent yields and selectivity. Besides, by detection or isolation of key intermediates, mechanism studies confirm that the deallylation undergoes η3-allylnickel intermediate pathway.

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