586-89-0
Chemical Structure
4-Acetylbenzoic acid
- CAS No.: 586-89-0
- Formula:C9H8O3
- Molecular Weight:164.16
IUPAC Name: 4-acetylbenzoic acid
InChIKey: QBHDSQZASIBAAI-UHFFFAOYSA-N
SMILES: O=C(O)C1=CC=C(C(C)=O)C=C1
Biological Activity: 4-Acetylbenzoic acid is a Zn(II) complex. 4-Acetylbenzoic acid is a derivative of benzoic acid that is commonly used in chemical synthesis. 4-Acetylbenzoic acid has an IC50 of 331.3 μM in murine L929 fibroblasts and an IC50 of 176 μM in metastatic melanoma B16 F10 cell lines[1][2][3].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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4-Acetylbenzoic acid | 99.76% | 4-Acetylbenzoic acid is a Zn(II) complex. 4-Acetylbenzoic acid is a derivative of benzoic acid that is commonly used in chemical synthesis. 4-Acetylbenzoic acid has an IC50 of 331.3 μM in murine L929 fibroblasts and an IC50 of 176 μM in metastatic melanoma B16 F10 cell lines. | ||||||||||||||||||||
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4-Acetylbenzoic acid (Standard) | ≥98% | 4-Acetylbenzoic acid (Standard) is the analytical standard of 4-Acetylbenzoic acid. This product is intended for research and analytical applications. 4-Acetylbenzoic acid is a Zn(II) complex. 4-Acetylbenzoic acid is a derivative of benzoic acid that is commonly used in chemical synthesis. 4-Acetylbenzoic acid has an IC50 of 331.3 μM in murine L929 fibroblasts and an IC50 of 176 μM in metastatic melanoma B16 F10 cell lines. | ||||||||||||||||||||
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- [1]. Nakamura R, et al. Selective oxidation of acetophenones bearing various functional groups to benzoic acid derivatives with molecular oxygen[J]. Advanced Synthesis & Catalysis, 2009, 351(10): 1677-1684.
- [2]. Wang L H, et al. Synthesis, Structural Characterization, DFT, Hirschfeld Surface and Catalytic Activity of a New Zn (II) Complex of 4-Acetylbenzoic Acid[J]. Bulletin of Chemical Reaction Engineering & Catalysis, 2023, 18(2): 200-209.
- [3]. Islam, A., et al., (2016). Cytotoxicity and apoptotic activity of novel organobismuth(V) and organoantimony(V) complexes in different cancer cell lines. European journal of medicinal chemistry, 109, 254–267. [Content Brief]