CAS 59430-62-5
:4-Amino-α-methylbenzeneacetic acid
Description:
4-Amino-α-methylbenzeneacetic acid, also known as 4-amino-α-methylphenylacetic acid, is an organic compound characterized by the presence of an amino group and a carboxylic acid functional group attached to a benzene ring. This compound features a methyl group adjacent to the amino group, which influences its solubility and reactivity. It typically appears as a white to off-white crystalline solid and is soluble in polar solvents such as water and alcohols, owing to the presence of the carboxylic acid group. The amino group can participate in hydrogen bonding, enhancing its interactions with other molecules. This compound may exhibit biological activity, making it of interest in pharmaceutical research and development. Its CAS number, 59430-62-5, is a unique identifier that facilitates the tracking and study of this substance in scientific literature and regulatory databases. As with many amino acids and their derivatives, it may play a role in various biochemical processes, although specific applications and mechanisms would depend on further research.
Formula:C9H11NO2
InChI:InChI=1S/C9H11NO2/c1-6(9(11)12)7-2-4-8(10)5-3-7/h2-6H,10H2,1H3,(H,11,12)
InChI key:InChIKey=WOMVICAMAQURRN-UHFFFAOYSA-N
SMILES:C(C(O)=O)(C)C1=CC=C(N)C=C1
Synonyms:- (+-)-2-(4-Aminophenyl)propionic acid
- (+-)-2-(p-Aminophenyl)propionic acid
- (+-)-alpha-(p-Aminophenyl)propionic acid
- 2-(4-Aminophenyl)Propanoic Acid
- 4-Amino-α-methylbenzeneacetic acid
- Benzeneacetic acid, 4-amino-alpha-methyl-, (+-)-
- Benzeneacetic acid, 4-amino-α-methyl-
- Hydratropic acid, p-amino-, (+-)-
- N-Deallylalminoprofen
- p-Amino-α-methylphenylacetic acid
- α-(4-Aminophenyl)-α-methylacetic acid
- α-(p-Aminophenyl)propionic acid
- See more synonyms
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Found 5 products.
2-(4-Aminophenyl)propanoic acid
CAS:<p>2-(4-Aminophenyl)propanoic acid</p>Purity:≥95%Color and Shape:SolidMolecular weight:165.18913g/mol2-(4-Aminophenyl)propanoic Acid
CAS:Controlled Product<p>Applications 2-(4-Aminophenyl)propanoic acid is a reagent in the preparation of 3-aminopyrazole inhibitors of CDK2/cyclin A as antitumor agents (Erratum).<br>References Pevarello, P., et al.: J. Med. Chem., 48, 5058 (2005);<br></p>Formula:C9H11NO2Color and Shape:NeatMolecular weight:165.192-(4-Aminophenyl)propanoic acid
CAS:<p>2-(4-Aminophenyl)propanoic acid (APPA) is an organic compound that is used in the synthesis of other chemicals. It can be synthesized by nitrating 4-aminophenol, which has a phenyl ring and a nucleophilic acetonitrile group. This reaction produces 2-nitrophenol, which can then be reduced to APPA. The nitro groups on APPA are cleaved by dithiothreitol and the reagents are deactivated by endogenous thiolates. Monitoring of these reactions is carried out using kinetic analysis.</p>Formula:C9H11NO2Purity:Min. 95%Molecular weight:165.19 g/mol




