3',4'-Dimethoxyacetophenone, 98%

Name: 3',4'-Dimethoxyacetophenone, 98% | 1131-62-0
Brand: J&K Chemical
SKU: JK425630_25_G
Price: 25.1 USD
Availability: InStock

Cat. No JK425630_25_G

Vendor: J&K Chemical

Product Information

Product Name

3',4'-Dimethoxyacetophenone, 98%

Brand Name

J&K

Product Number

425630

CAS

1131-62-0

Molecular Formula

C10H12O3

Molecular Weight

180.20

SDS Document

View/Download

Certificate of Analysis (COA)

COA not found

General Information

Synonyms

4-Acetylveratrole

PubChem CID

14328

IUPAC Name

1-(3,4-dimethoxyphenyl)ethanone

InChI Key

IQZLUWLMQNGTIW-UHFFFAOYSA-N

SMILES

CC(=O)C1=CC(=C(C=C1)OC)OC

Properties

Melting Point

47-54

Boiling Point

286-288

Flash Point

>113

Safety Information

Precautionary Statement

P262

References Data Source From Pubchem

Reactions with Allenes

Publication Name: Science of Synthesis

Publication Date: 2026

Reactions with Alkenes

Publication Name: Science of Synthesis

Publication Date: 2026

Metal-Free Sustainable N-α-C(sp3)-H Functionalization of Arylmethylamines with Arylmethylketones to Synthesis of Kröhnke Pyridines Under Solvent-free Condition

Publication Name: Catalysis Letters

Publication Date: 2024-12-02

DOI: 10.1007/s10562-024-04873-x

Investigating novel tubulin polymerization inhibitors: design, synthesis, LC/MS cellular permeability, in silico studies, and in vitro assessment

Publication Name: Medicinal Chemistry Research

Publication Date: 2024-11-11

DOI: 10.1007/s00044-024-03327-8

Effects of the structure of primary nitroalkanes and reaction conditions on the selectivity of acylamination of arenes in polyphosphoric acid

Publication Name: Russian Chemical Bulletin

Publication Date: 2024-06

DOI: 10.1007/s11172-024-4277-8

3',4'-Dimethoxyacetophenone, 98%

Product Information

General Information

Properties

Safety Information

References Data Source From Pubchem

Reactions with Allenes

Reactions with Alkenes

Metal-Free Sustainable N-α-C(sp3)-H Functionalization of Arylmethylamines with Arylmethylketones to Synthesis of Kröhnke Pyridines Under Solvent-free Condition

Investigating novel tubulin polymerization inhibitors: design, synthesis, LC/MS cellular permeability, in silico studies, and in vitro assessment

Effects of the structure of primary nitroalkanes and reaction conditions on the selectivity of acylamination of arenes in polyphosphoric acid