1189708-92-6
1189708-92-6
Chemical Structure
2-Phenylbutyric acid-d5
- CAS No.: 1189708-92-6
- Formula:C10H7D5O2
- Molecular Weight:169.23
IUPAC Name: 2-phenylbutanoic-3,3,4,4,4-d5 acid
InChIKey: OFJWFSNDPCAWDK-ZBJDZAJPSA-N
SMILES: OC(C(C1=CC=CC=C1)C([2H])([2H])C([2H])([2H])[2H])=O
Biological Activity: 2-Phenylbutyric acid-d5 is the deuterium labeled 2-Phenylbutanoic acid (HY-W017194). 2-Phenylbutanoic acid is a monocarboxylic acid. 2-Phenylbutanoic acid interacts with proteins. 2-Phenylbutanoic acid is used in the study of malignant lymphoma and HIV virus-related diseases[1][2].
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2-Phenylbutyric acid-d5 | 2-Phenylbutyric acid-d5 is the deuterium labeled 2-Phenylbutanoic acid (HY-W017194). 2-Phenylbutanoic acid is a monocarboxylic acid. 2-Phenylbutanoic acid interacts with proteins. 2-Phenylbutanoic acid is used in the study of malignant lymphoma and HIV virus-related diseases. | |||||||||||||||||||||
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2-Phenylbutanoic acid (Standard) | ≥98% | 2-Phenylbutanoic acid (Standard) is the analytical standard of 2-Phenylbutanoic acid. This product is intended for research and analytical applications. 2-Phenylbutanoic acid is a monocarboxylic acid. 2-Phenylbutanoic acid interacts with proteins. 2-Phenylbutanoic acid is used in the study of malignant lymphoma and HIV virus-related diseases。 | ||||||||||||||||||||
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2-Phenylbutanoic acid-d3 | 2-Phenylbutanoic acid-d3 is the deuterium labeled 2-Phenylbutanoic acid (HY-W017194). 2-Phenylbutanoic acid is a monocarboxylic acid. 2-Phenylbutanoic acid interacts with proteins. 2-Phenylbutanoic acid is used in the study of malignant lymphoma and HIV virus-related diseases. | |||||||||||||||||||||
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2-Phenylbutanoic acid | 99.90% | 2-Phenylbutanoic acid is a monocarboxylic acid. 2-Phenylbutanoic acid interacts with proteins. 2-Phenylbutanoic acid is used in the study of malignant lymphoma and HIV virus-related diseases. | ||||||||||||||||||||
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References
- [1]. Raajaraman B R, et al. Influence of acetyl, hydroxy and methyl functional groups on 2-phenylbutanoic acid by quantum computational, spectroscopic and ligand-protein docking studies. Journal of Molecular Structure, 2019, 1188: 99-109.
- [2]. Yamada H, et al. Comparison of 1-octanol with benzene in the extraction of copper (II) with various phenylcarboxylic acids. Analytical sciences, 1999, 15(8): 773-780.
