4-Methoxyacetophenone - ≥99%, used for 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 approv

CAS: 100-06-1 Cat. No.: M103875 Formula: C₉H₁₀O₂ Peso molecolare: 150.17 Beilstein Registry Number: 742313 Numero EC: 202-815-9

GRADE & PURITY ≥99%

Synonyms

1-(4-methoxyphenyl)ethan-1-one | 4'-Methoxyacetophenone | P-ACETYLANISOLE | 1-(4-Methoxyphenyl)ethanone | Linarodin | Acetanisole | p-Methoxyacetophenone | Vananote | 4-Acetylanisole | 4-Acetoanisole | Novatone

Storage

Store at 2-8°C

Shipped In

Wet ice

Panoramica

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.

Specifications

Sinonimi

1-(4-methoxyphenyl)ethan-1-one | 4'-Methoxyacetophenone | P-ACETYLANISOLE | 1-(4-Methoxyphenyl)ethanone | Linarodin | Acetanisole | p-Methoxyacetophenone | Vananote | 4-Acetylanisole | 4-Acetoanisole | Novatone

Specifiche e purezza

≥99%

Applicazione

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 Clostridiu

Condizioni di conservazione di stoccaggio

Store at 2-8°C

Spedito in

Wet ice

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Purezza

≥99%

Nomi e identificatori

• Pubchem Sid: 504751356
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504751356
• Sorrisi canonici: CC(=O)C1=CC=C(C=C1)OC
• IUPAC Name: 1-(4-methoxyphenyl)ethanone
• InChIKey: NTPLXRHDUXRPNE-UHFFFAOYSA-N
• INCHI: 1S/C9H10O2/c1-7(10)8-3-5-9(11-2)6-4-8/h3-6H,1-2H3
• Isomeri SMILES: CC(=O)C1=CC=C(C=C1)OC
• WGK Germania: 2
• RTECS: AM9240000
• Peso molecolare: 150.17
• Beilstein: 742313
• Reaxy-Rn: 742313
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=742313&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic oxygen compounds
    • Classe Organooxygen compounds
      • Subclass Carbonyl compounds
        • Level5 Ketones
          • Level6 Aryl ketones
            • Level7 Phenylketones
              • Level8 Alkyl-phenylketones

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Classe: Organooxygen compounds
• Subclass: Carbonyl compounds
• Intermediate Tree Nodes: Ketones - Aryl ketones - Phenylketones
• Direct Parent: Alkyl-phenylketones
• Alternative Parents: Acetophenones Phenoxy compounds Methoxybenzenes Benzoyl derivatives Aryl alkyl ketones Anisoles Alkyl aryl ethers Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Alkyl-phenylketone - Acetophenone - Phenoxy compound - Methoxybenzene - Aryl alkyl ketone - Phenol ether - Benzoyl - Anisole - Alkyl aryl ether - Benzenoid - Monocyclic benzene moiety - Ether - Organic oxide - Hydrocarbon derivative - Aromatic homomonocyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as alkyl-phenylketones. These are aromatic compounds containing a ketone substituted by one alkyl group, and a phenyl group.
• External Descriptors: monomethoxybenzene - acetophenones

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

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Meccanismi d'azione

Proprietà chimiche e fisiche

• Solubilità: Soluble in Methanol
• Sensibilità: heat & Light sensitive.
• Punto di infiammabilità (°F): 280.4 °F
• Punto di infiammabilità (°C): 138 °C
• Punto di ebollizione (°C): 152-154°C
• Punto di fusione (°C): 36-38°C
• Peso molecolare: 150.170 g/mol
• XLogP3: 1.700
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 2
• Exact Mass: 150.068 Da
• Monoisotopic Mass: 150.068 Da
• Topological Polar Surface Area: 26.300 Ų
• Heavy Atom Count: 11
• Formal Charge: 0
• Complexity: 134.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

Riferimenti

1. Nian Wang, Die Zhou, Huaying Liu, Yina Tu, Yanqiong Ma, Yingjie Li.  (2023)  Triplet-Excited Dissolved Organic Matter Efficiently Promoted Atmospheric Sulfate Production: Kinetics and Mechanisms.  Separations,  10  (6): (335).  [PMID:] [10.3390/separations10060335]

2. Shuibo Wang, Chunzheng Wu, Hongbo Yu, Yuting Chu, Shiwei Wang, Tong Li, Hongfeng Yin.  (2022)  Tuning the catalytic performance of Pt/SiO2 catalysts by CoOx modification for selective hydrogenations of unsaturated carbonyl compounds.  APPLIED SURFACE SCIENCE,      [PMID:] [10.1016/j.apsusc.2022.154867]

3. Huiqing Luo, Na Li, Liyan Liu, Huaqiao Wang, Feng He.  (2021)  Synthesis of New AIEE-Active Chalcones for Imaging of Mitochondria in Living Cells and Zebrafish In Vivo.  INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES,  22  (16): (8949).  [PMID:34445653] [10.3390/ijms22168949]

4. Liyun Huang, Kui Wu, Qian He, Chao Xiong, Tao Gan, Xiaohui He, Hongbing Ji.  (2021)  Quasi-continuous synthesis of iron single atom catalysts via a microcapsule pyrolysis strategy.  AICHE JOURNAL,  67  (6): (e17197).  [PMID:] [10.1002/aic.17197]

5. Nengchao Luo, Tingting Hou, Shiyang Liu, Bin Zeng, Jianmin Lu, Jian Zhang, Hongji Li, Feng Wang.  (2019)  Photocatalytic Coproduction of Deoxybenzoin and H2 through Tandem Redox Reactions.  ACS Catalysis,      [PMID:] [10.1021/acscatal.9b03651]

6. Bin Chen, Jun Hu, Zhihao Yu, Lin Zhu, Chunzheng Wu, Hongbo Yu.  (2025)  Improving the Activity and Selectivity of Ir/SiO2 for the Selective Hydrogenation of Unsaturated Carbonyl Compounds by SnO2 Promotion.  INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH,      [PMID:] [10.1021/acs.iecr.4c04318]

7. Yifan Zhang, Jiaying Liu, Shiwei Wang, Zhihao Yu, Haojian Zhang, Dong Wang, Lin Zhu, Chunzheng Wu, Hongbo Yu.  (2025)  Enhanced Selective Hydrogenation of Acetophenone over KIT-6 Supported Pd-MO x (M = Fe, Co, Ni) Hybrid Nanostructures.  Catalysis Science & Technology,      [PMID:] [10.1039/D5CY01108F]

8. Jun Zhang, Ying Qiu, Chengyu Li, Rui Shan, Haoran Yuan, Yong Chen.  (2026)  Antibiotic residues derived carbonaceous materials for transfer hydrogenation of bio-based furfural: experiments, kinetics and techno-economic analysis.  ENERGY,      [PMID:] [10.1016/j.energy.2026.140482]