90-27-7
90-27-7
Chemical Structure
2-Phenylbutanoic acid
- CAS No.: 90-27-7
- Formula:C10H12O2
- Molecular Weight:164.20
IUPAC Name: 2-phenylbutanoic acid
InChIKey: OFJWFSNDPCAWDK-UHFFFAOYSA-N
SMILES: CCC(C1=CC=CC=C1)C(O)=O
Biological Activity: 2-Phenylbutanoic acid is a sterically hindered carboxylic acid. 2-Phenylbutanoic acid exhibits anticancer activity through molecular docking interactions with cytochrome P450 proteins. 2-Phenylbutanoic acid can be used in research on malignant lymphoma[1][2][3].
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2-Phenylbutanoic acid | 99.90% | 2-Phenylbutanoic acid is a sterically hindered carboxylic acid. 2-Phenylbutanoic acid exhibits anticancer activity through molecular docking interactions with cytochrome P450 proteins. 2-Phenylbutanoic acid can be used in research on malignant lymphoma. | ||||||||||||||||||||
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2-Phenylbutanoic acid (Standard) | ≥98% | 2-Phenylbutanoic acid (Standard) is the analytical standard of 2-Phenylbutanoic acid (HY-W017194). This product is intended for research and analytical applications. 2-Phenylbutanoic acid is a sterically hindered carboxylic acid. 2-Phenylbutanoic acid exhibits anticancer activity through molecular docking interactions with cytochrome P450 proteins. 2-Phenylbutanoic acid can be used in research on malignant lymphoma. | ||||||||||||||||||||
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2-Phenylbutyric acid-d5 | 2-Phenylbutyric acid-d5 is the deuterated-labeled 2-Phenylbutanoic acid (HY-W017194). 2-Phenylbutanoic acid is a sterically hindered carboxylic acid. 2-Phenylbutanoic acid exhibits anticancer activity through molecular docking interactions with cytochrome P450 proteins. 2-Phenylbutanoic acid can be used in research on malignant lymphoma. | |||||||||||||||||||||
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2-Phenylbutanoic acid-d3 | 2-Phenylbutanoic acid-d3 is the deuterated-labeled 2-Phenylbutanoic acid (HY-W017194). 2-Phenylbutanoic acid is a sterically hindered carboxylic acid. 2-Phenylbutanoic acid exhibits anticancer activity through molecular docking interactions with cytochrome P450 proteins. 2-Phenylbutanoic acid can be used in research on malignant lymphoma. | |||||||||||||||||||||
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Thiomandelic acid | 95.37% | Thiomandelic acid is a broad spectrum inhibitor of Zinc -lactamases. | ||||||||||||||||||||
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2-Phenylglycine | 98.70% | 2-Phenylglycine (DL-α-Phenylglycine) is a metabolite in breast milk during the W2 to W4 lactation period. | ||||||||||||||||||||
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Mandelic acid (Standard) | 99.84% | Mandelic acid (Standard) is the analytical standard of Mandelic acid. This product is intended for research and analytical applications. Mandelic acid ((±)-Mandelic acid), an alpha-hydroxycarboxylic acid, has been widely used as an intermediate of pharmaceutical and fine chemicals. Mandelic acid shows antimicrobial activity and has been used for the research of urinary tract infections and vaginal trichomoniasis. Mandelic acid exhibits high sperm-immobilizing activity and low vaginal irritation. | ||||||||||||||||||||
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2-Phenylpropionic acid | 99.70% | 2-Phenylpropionic acid is an intermediate in the metabolism of alpha-Methylstyrene. 2-Phenylpropionic acid covalently binds to rat liver protein. 2-Phenylpropionic acid can be used in the research of nonsteroidal anti-inflammatory agents. | ||||||||||||||||||||
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3-Phenylbutyric acid (Standard) | ≥98% | 3-Phenylbutyric acid is metabolized by initial oxidation of the benzene ring and by initial oxidation of the side chain. 3-Phenylbutyric acid can be used to isolate Rhodococcus rhodochrous PB1 from compost soil. | ||||||||||||||||||||
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Tropic acid | 99.81% | Tropic acid (DL-Tropic acid) is an active small molecule that can be used as the pharmaceutical intermediate. | ||||||||||||||||||||
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Indobufen impurity 16 | Indobufen impurity 16 is an impurity of Indobufen (HY-18763). | |||||||||||||||||||||
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Mandelic Acid-13C8 | 98.17% | Mandelic Acid-13C8 ((±)-Mandelic acid-13C8) is the 13C-labeled Mandelic acid (HY-W015591). Mandelic acid ((±)-Mandelic acid), an alpha-hydroxycarboxylic acid, has been widely used as an intermediate of pharmaceutical and fine chemicals. Mandelic acid shows antimicrobial activity and has been used for the research of urinary tract infections and vaginal trichomoniasis. Mandelic acid exhibits high sperm-immobilizing activity and low vaginal irritation. | ||||||||||||||||||||
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D-(-)-Mandelic acid | 99.92% | D-(-)-Mandelic acid is an orally active alpha hydroxycarboxylic acid that can be isolated from bitter almonds and Indian chestnut trees. It has antioxidant and antibacterial properties and is expected to play an important role in the treatment of rheumatoid arthritis. | ||||||||||||||||||||
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(S)-Mandelic acid | 99.75% | (S)-Mandelic Acid is a (S)-enantiomer of Mandelic Acid (HY-W015591). (S)-Mandelic Acid undergoes one-directional chiral inversion to (R)-Mandelic Acid in rat models. (S)-Mandelic acid is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | ||||||||||||||||||||
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References
- [1]. Cavallaro PA, et al. Titanium Tetrachloride-Assisted Direct Esterification of Carboxylic Acids. Molecules (Basel, Switzerland). 2024 Feb 08;29(4):777.
- [2]. Kodama K, et al. Application of threo-2-amino-1,2-diphenylethanol as a Resolving Agent for Racemic Carboxylic Acids via Diastereomeric Salt Formation. Chirality. 2026 Sep;38(9):e70149.
- [3]. Raajaraman BR, et al. Influence of acetyl, hydroxy and methyl functional groups on 2‑phenylbutanoic acid by quantum computational, spectroscopic and ligand‑protein docking studies. J Mol Struct. 2019;1188:99‑109.
