2-(Allyloxy)benzoic acid, 97%

Name: 2-(Allyloxy)benzoic acid, 97% | 59086-52-1
Brand: J&K Chemical
SKU: JK511166_25_G
Price: 769.4 USD
Availability: OutOfStock

Cat. No JK511166_25_G

Vendor: J&K Chemical

Product Information

Product Name

2-(Allyloxy)benzoic acid, 97%

Brand Name

J&K

Product Number

511166

CAS

59086-52-1

Molecular Formula

C10H10O3

Molecular Weight

178.19

Certificate of Analysis (COA)

COA not found

General Information

PubChem CID

3798703

IUPAC Name

2-prop-2-enoxybenzoic acid

InChI Key

XPWMIGFSEWFXEZ-UHFFFAOYSA-N

SMILES

C=CCOC1=CC=CC=C1C(=O)O

References

Enhancement of thermal and mechanical performances of epoxy nanocomposite materials based on graphene oxide grafted by liquid crystalline monomer with Schiff base

Publication Name: Journal of Materials Science

Publication Date: 2019-12-11

DOI: 10.1007/s10853-019-04273-2

Acyl Radical Chemistry via Visible-Light Photoredox Catalysis

Publication Name: Synthesis

Publication Date: 2018-12-12

DOI: 10.1055/s-0037-1610329

Facile Synthesis of 2,3-Dihydrobenzofuran-3-ylacetic Acids by Novel Electrochemical Sequential Aryl Radical Cyclization–Carboxylation of 2-Allyloxybromobenzenes Using Methyl 4-tert-Butylbenzoate as an Electron-Transfer Mediator

Publication Name: Synlett

Publication Date: 2011-06-15

DOI: 10.1055/s-0030-1260794

Facile and Selective Deallylation of Allyl Ethers Using Diphosphinidenecyclobutene-Coordinated Palladium Catalysts

Publication Name: The Journal of Organic Chemistry

Publication Date: 2004-05-26

DOI: 10.1021/jo049732q

2-(Allyloxy)benzoic acid, 97%

Product Information

General Information

References

Enhancement of thermal and mechanical performances of epoxy nanocomposite materials based on graphene oxide grafted by liquid crystalline monomer with Schiff base

Acyl Radical Chemistry via Visible-Light Photoredox Catalysis

Facile Synthesis of 2,3-Dihydrobenzofuran-3-ylacetic Acids by Novel Electrochemical Sequential Aryl Radical Cyclization–Carboxylation of 2-Allyloxybromobenzenes Using Methyl 4-tert-Butylbenzoate as an Electron-Transfer Mediator

Facile and Selective Deallylation of Allyl Ethers Using Diphosphinidenecyclobutene-Coordinated Palladium Catalysts