3334-67-6

Basic information

• Product Name: 3-[(3-methoxyphenyl)amino]propanoic acid
• Synonyms: 3-[(3-methoxyphenyl)amino]propanoic acid;B-ALANINE, N-(3-METHOXYPHENYL)-;N-(3-METHOXYPHENYL)-B-ALANINE;OTAVA-BB 1142588
• CAS NO: 3334-67-6
• Molecular Formula: C₁₀H₁₃NO₃
• Molecular Weight: 195.22
• Mol File: 3334-67-6.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 140-145 °C(Press: 0.2 Torr)
• Appearance: /
• Density: 1.216±0.06 g/cm3(Predicted)
• PKA: 3.58±0.12(Predicted)
• CAS DataBase Reference: 3-[(3-methoxyphenyl)amino]propanoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 3-[(3-methoxyphenyl)amino]propanoic acid(3334-67-6)
• EPA Substance Registry System: 3-[(3-methoxyphenyl)amino]propanoic acid(3334-67-6)

Safety Data

• Hazardous Substances Data: 3334-67-6(Hazardous Substances Data)

Usage

Description

3-[(3-methoxyphenyl)amino]propanoic acid is an amino acid derivative with the molecular formula C11H15NO4. It features a methoxyphenyl group attached to the amino group of the amino acid propanoic acid, giving it both acidic and basic functional groups. This amphoteric nature allows it to act as both an acid and a base, and its potential applications in pharmaceuticals are of interest due to the importance of amino acids in protein synthesis and various physiological processes in the human body.

Uses

Used in Pharmaceutical Industry:
3-[(3-methoxyphenyl)amino]propanoic acid is used as a building block for protein synthesis and may have potential applications in drug development. Its unique structure, including the methoxyphenyl group, could impart specific chemical and biological properties that are valuable for creating new pharmaceutical agents or enhancing existing ones. 3-[(3-methoxyphenyl)amino]propanoic acid's amphoteric nature may also contribute to its versatility in medicinal chemistry.

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Relevant articles and documents

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The invention discloses 2,3-dihydro-1H-quinoline-4-ketone thiosemicarbazone derivatives as well as a preparation method and application thereof. The structural formula of the derivatives is as shown in a formula (I): (the formula is as shown in the description), wherein R1 is halogen, alkyl or alkoxy; R2 is hydrogen, halogen or alkoxy; R3 is hydrogen or halogen; R4 is hydrogen or halogen; X is hydrogen, acetyl or nitryl; and Y is hydrogen or phenyl. The derivatives can obviously inhibit proliferation of tumor cells, and has significant inhibition effect on multiple cancer cell strains such asbreast cancer cells, melanoma cells and prostatic cancer cells; and the anti-tumor activity is obviously better than that of a broad-spectrum anti-cancer medicine cis-platinum. In addition, the preparation process of the derivatives is simple, the conditions are mild, the sources of the raw materials are rich, the production cost is low, and potential medicinal value and good application prospectin the aspect of preparing a novel anti-tumor medicine are achieved.

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