4'-Butylacetophenone, 99%

Name: 4'-Butylacetophenone, 99% | 37920-25-5
Brand: J&K Chemical
SKU: JK335160_5_G
Price: 18.9 USD
Availability: OutOfStock

Cat. No JK335160_5_G

Vendor: J&K Chemical

Product Information

Product Name

4'-Butylacetophenone, 99%

Brand Name

J&K

Product Number

335160

CAS

37920-25-5

Molecular Formula

C12H16O

Molecular Weight

176.25

SDS Document

View/Download

Certificate of Analysis (COA)

COA not found

General Information

Synonyms

1-(4-butylphenyl)-ethanon
Ethanone
1-(4-butylphenyl)-
1-(4-Butylphenyl)ethan-1-one

PubChem CID

123470

IUPAC Name

1-(4-butylphenyl)ethanone

InChI Key

MQESVSITPLILCO-UHFFFAOYSA-N

SMILES

CCCCC1=CC=C(C=C1)C(=O)C

Properties

Density

0.957

Boiling Point

101-102

Flash Point

>113

n20D

1.517

References Data Source From Pubchem

Benzylic C—H Fluorination

Publication Name: Science of Synthesis

Publication Date: 2025

Silylmethyl Groups as Ligands on Metals

Publication Name: Science of Synthesis

Publication Date: 2022

Generating the Blood Exposome Database Using a Comprehensive Text Mining and Database Fusion Approach

Publication Name: Environmental Health Perspectives

Publication Date: 2019-09-01

DOI: 10.1289/ehp4713

Substantiation of the Selection of Trifluoroacetophenone Derivatives for the Manufacture of Membranes of Sulfate- and Carbonate-Selective Electrodes

Publication Name: Journal of Analytical Chemistry

Publication Date: 2019-08-09

DOI: 10.1134/s1061934819080124

Iron-Catalysed Aerobic Oxidative C–C Bond Cleavage of Ketones for the Synthesis of Primary Amides

Publication Name: SynOpen

Publication Date: 2019-01

DOI: 10.1055/s-0037-1611676

4'-Butylacetophenone, 99%

Product Information

General Information

Properties

References Data Source From Pubchem

Benzylic C—H Fluorination

Silylmethyl Groups as Ligands on Metals

Generating the Blood Exposome Database Using a Comprehensive Text Mining and Database Fusion Approach

Substantiation of the Selection of Trifluoroacetophenone Derivatives for the Manufacture of Membranes of Sulfate- and Carbonate-Selective Electrodes

Iron-Catalysed Aerobic Oxidative C–C Bond Cleavage of Ketones for the Synthesis of Primary Amides