117374

4′-Methoxyacetophenone

99%

• Sinónimos: 4-Acetylanisole
• Fórmula lineal: CH₃OC₆H₄COCH₃
• Número de CAS: 100-06-1
• Peso molecular: 150.17
• Beilstein/REAXYS Number: 742313
• EC Number: 202-815-9
• MDL number: MFCD00008745
• UNSPSC Code: 12352100
• eCl@ss: 39023808
• PubChem Substance ID: 24847327
• NACRES: NA.22

Propiedades

• Quality Level: 200
• assay: 99%
• form: solid
• bp: 152-154 °C/26 mmHg (lit.)
• mp: 36-38 °C (lit.)
• solubility: H₂O: soluble 2.474 g/L at 20 °C
• functional group: ketone
• SMILES string: COc1ccc(cc1)C(C)=O
• InChI: 1S/C9H10O2/c1-7(10)8-3-5-9(11-2)6-4-8/h3-6H,1-2H3
• InChI key: NTPLXRHDUXRPNE-UHFFFAOYSA-N

Descripción

General description

4′-Methoxyacetophenone undergoes biocatalytic enantioselective reduction using immobilized Rhodotorula sp. AS2.2241 cells to yield (S)-1-(4-methoxyphenyl) ethanol in a hydrophilic ionic liquid-containing co-solvent system.

Application

4′-Methoxyacetophenone was used to study ruthenium catalyzed step growth copolymerization of 4′-methoxyacetophenone with α,ω-dienes to yield copolymers. It was used to determine the activity of various ketones approved as food additives against Clostridium Botulinum spores and cells.

Información de seguridad

• pictograms: GHS07
• signalword: Warning
• hcodes: H302
• pcodes: P264 - P270 - P301 + P312 - P501
• Hazard Classifications: Acute Tox. 4 Oral
• Storage Class: 11 - Combustible Solids
• wgk_germany: WGK 1
• flash_point_f: 280.4 °F - open cup
• flash_point_c: 138 °C - open cup
• ppe: dust mask type N95 (US), Eyeshields, Gloves