CAS 746672-87-7

4-Pyridinepropanoicacid, a-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-(9CI)

Description:

4-Pyridinepropanoic acid, a-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-(9CI), commonly referred to as Fmoc-4-pyridinepropanoic acid, is a chemical compound characterized by its structure, which includes a pyridine ring and a fluorenylmethoxycarbonyl (Fmoc) protecting group. This compound is typically used in peptide synthesis as a building block due to its ability to protect amino groups during the coupling process. The presence of the pyridine moiety contributes to its unique reactivity and solubility properties, making it suitable for various organic synthesis applications. The Fmoc group is particularly advantageous because it can be easily removed under mild basic conditions, allowing for the selective deprotection of amino acids. Additionally, this compound may exhibit specific interactions with biological targets, making it of interest in medicinal chemistry and drug development. Its CAS number, 746672-87-7, allows for easy identification and retrieval of information related to its properties and applications in scientific literature.

Formula: C₂₃H₂₀N₂O₄

Synonyms:

• Fmoc-3-(4-Pyridyl)-Dl-Alanine

Fmoc-dl-4-pyridylalanine

CAS: 746672-87-7

Formula: C₂₃H₂₀N₂O₄

Purity: 95%

Color and Shape: Solid

Molecular weight: 388.4159

Ref: IN-DA005A6N

FMOC-DL-4-Pyridylalanine

CAS: 746672-87-7

FMOC-DL-4-Pyridylalanine

Purity: 95%

Molecular weight: 388.42g/mol

Ref: 54-OR303875

Fmoc-DL-4-pyridylalanine

CAS: 746672-87-7

Versatile small molecule scaffold

Formula: C₂₃H₂₀N₂O₄

Purity: Min. 95%

Molecular weight: 388.42 g/mol

Ref: 3D-WEB67287