4-Benzyloxy-2-hydroxyacetophenone, 97%

Name: 4-Benzyloxy-2-hydroxyacetophenone, 97% | 29682-12-0
Brand: J&K Chemical
SKU: JK770458_25_G
Price: 109.8 USD
Availability: OutOfStock

Cat. No JK770458_25_G

Vendor: J&K Chemical

Product Information

Product Name

4-Benzyloxy-2-hydroxyacetophenone, 97%

Brand Name

J&K

Product Number

770458

CAS

29682-12-0

Molecular Formula

C15H14O3

Molecular Weight

242.27

Certificate of Analysis (COA)

COA not found

General Information

Synonyms

1-(4-(Benzyloxy)-2-hydroxyphenyl)ethanone
2-Hydroxy-4-benzyloxyacetophenone

PubChem CID

309257

IUPAC Name

1-(2-hydroxy-4-phenylmethoxyphenyl)ethanone

InChI Key

AGQNLHOTLJFJCG-UHFFFAOYSA-N

SMILES

CC(=O)C1=C(C=C(C=C1)OCC2=CC=CC=C2)O

Properties

Melting Point

103-107

Boiling Point

415.7

References Data Source From Pubchem

Discovery of C-3 isoxazole substituted thiochromone S,S-dioxide derivatives as potent and selective inhibitors for monoamine oxidase B (MAO-B)

Publication Name: European Journal of Medicinal Chemistry

Publication Date: 2024-01-05

DOI: 10.1016/j.ejmech.2023.115956

Synthesis and neuroprotective activity of a (–)-cytisine-isoflavone conjugate

Publication Name: Chemistry of Heterocyclic Compounds

Publication Date: 2023-02

DOI: 10.1007/s10593-023-03160-8

Condensation of 2-Hydroxyacetophenones with Carbonyl Compounds

Publication Name: Science of Synthesis

Publication Date: 2019

Defining a minimum pharmacophore for simocyclinone D8 disruption of DNA gyrase binding to DNA

Publication Name: Medicinal Chemistry Research

Publication Date: 2014-02-20

DOI: 10.1007/s00044-014-0942-z

Synthesis of benzo[b]furan-2-thioles from 4-(2-hydroxyaryl)-1,2,3-thiadiazoles

Publication Name: Russian Journal of Organic Chemistry

Publication Date: 2012-05

DOI: 10.1134/s1070428012050168

4-Benzyloxy-2-hydroxyacetophenone, 97%

Product Information

General Information

Properties

References Data Source From Pubchem

Discovery of C-3 isoxazole substituted thiochromone S,S-dioxide derivatives as potent and selective inhibitors for monoamine oxidase B (MAO-B)

Synthesis and neuroprotective activity of a (–)-cytisine-isoflavone conjugate

Condensation of 2-Hydroxyacetophenones with Carbonyl Compounds

Defining a minimum pharmacophore for simocyclinone D8 disruption of DNA gyrase binding to DNA

Synthesis of benzo[b]furan-2-thioles from 4-(2-hydroxyaryl)-1,2,3-thiadiazoles