CAS 109579-23-9: BOC-(3S,4S)-4-AMINO-3-HYDROXY-5-(3-INDOLYL)-PENTANOIC ACID

Description: BOC-(3S,4S)-4-AMINO-3-HYDROXY-5-(3-INDOLYL)-PENTANOIC ACID, with the CAS number 109579-23-9, is a synthetic amino acid derivative characterized by its unique structural features. It contains a tert-butyloxycarbonyl (BOC) protecting group, which is commonly used in peptide synthesis to protect the amino group. The compound exhibits chirality, with specific stereochemistry at the 3 and 4 positions, contributing to its potential biological activity. The presence of an indole moiety enhances its pharmacological properties, making it of interest in medicinal chemistry, particularly in the development of neuroactive compounds. This substance is soluble in polar organic solvents and may exhibit varying solubility in water, depending on pH. Its functional groups suggest potential interactions with biological targets, making it a candidate for further research in drug development and biochemical applications. As with many amino acid derivatives, it may also participate in various chemical reactions, including coupling reactions for peptide synthesis.

Formula: C₁₈H₂₄N₂O₅

Synonyms:

• Boc-Ahipa
• Boc-Ahipa-Oh

L-threo-Pentonic acid,2,4,5-trideoxy-4-[[(1,1-dimethylethoxy)carbonyl]amino]-5-(1H-indol-3-yl)-

CAS: 109579-23-9

• Formula: C₁₈H₂₄N₂O₅
• Molecular weight: 348.3936

Boc-(3S,4S)-4-amino-3-hydroxy-5-(3-indolyl)pentanoic acid

CAS: 109579-23-9

• Purity: 97.0%
• Molecular weight: 348.39898681640625

Boc-(3S,4S)-4-amino-3-hydroxy-5-(3-indolyl)pentanoic acid

CAS: 109579-23-9

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• Formula: C₁₈H₂₄N₂O₅
• Purity: Min. 95%
• Molecular weight: 348.39 g/mol