151414-76-5

Basic information

• Product Name: 2-Allyloxyphenylboronic acid
• Synonyms: 2-Allyloxyphenylboronic acid
• CAS NO: 151414-76-5
• Molecular Formula: C₉H₁₁BO₃
• Molecular Weight: 177.99284
• Mol File: 151414-76-5.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 351.8±44.0 °C(Predicted)
• Appearance: /
• Density: 1.12±0.1 g/cm3(Predicted)
• PKA: 8.59±0.53(Predicted)
• CAS DataBase Reference: 2-Allyloxyphenylboronic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Allyloxyphenylboronic acid(151414-76-5)
• EPA Substance Registry System: 2-Allyloxyphenylboronic acid(151414-76-5)

Safety Data

• Hazardous Substances Data: 151414-76-5(Hazardous Substances Data)

Usage

General Description

2-Allyloxyphenylboronic acid is a chemical compound with the molecular formula C9H11BO3. It is a boronic acid derivative that contains both a boronic acid functional group and an allyloxy functional group, which can facilitate its use as a building block in organic synthesis. 2-Allyloxyphenylboronic acid has been used in the development of various pharmaceuticals and agrochemicals, as well as in the preparation of materials for organic electronic devices. Its versatile reactivity and potential applications make it a valuable tool in the field of organic chemistry.

Upstream product

• 5419-55-6 Triisopropyl borate 
• 60333-75-7 O-allyl-2-bromophenol 
• 61676-62-8 2-Isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 24892-63-5 1-allyloxy-2-iodobenzene 

Downstream Products

• 1242412-59-4 C₁₈H₁₈O₂ 
• 6282-42-4 methyl 2-allyloxybenzoate 
• 73429-23-9 2,2′-di(allyloxy)-biphenyl 
• 89844-08-6 prop-2-enyl 2-prop-2-enoxybenzoate 
• 151414-77-6 o-(Prop-2-enyloxy)phenyllead Triacetate 
• 3383-05-9 allyl 2-allylphenyl ether 
• 1334402-71-9 2-(benzofuran-3-ylmethyl)cyclohexa-2,5-diene-1,4-dione 
• 1334402-70-8 2-((2,3-dihydrobenzofuran-3-yl)methyl)cyclohexa-2,5-diene-1,4-dione 

Relevant articles and documents

1,4-Phenylene-bis-((1-methyl-1H-pyrazol-5-yl)borinic 8-oxyquinolinate) as a photoredox catalyst in the atom transfer radical addition of iodoperfluoroalkanes to alkenyl groups bearing organoboron compounds

The key photocatalytic properties of a transition-metal-free heteroleptic complex derived from 1,4-phenyldiboronic acid were evaluated. This compound was utilized in the atom transfer radical addition of iodoperfluoroalkanes to a series of alkenyl group b

Mechanism of Arylation of Nucleophiles by Aryllead Triacetates. Part 1. Exclusion of a Pathway involving Aryl Free Radicals

o-(Prop-2-enyloxy)phenyllead triacetate 6, which was obtained by treatment of the corresponding boronic acid with lead tetraacetate, has been shown to react with iodide and azide ions, 2,4,6-trimethylphenol, ethyl 2-oxocyclopentanecarboxylate, and the sodium salt of 2-nitropropane to give only those products which, in a formal sense, are derived by direct nucleophilic displacement of the Pb(OAc)3 group.The complete absence of 3-substituted dihydrobenzofurans among the products is strong evidence that aryl free radicals are not involved in the arylation reactions of aryllead triacetates.