CAS 142855-79-6

1H-Azepine-1-aceticacid,3-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]hexahydro-2-oxo-,(3S)-(9CI)

Description:

1H-Azepine-1-acetic acid, 3-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]hexahydro-2-oxo-, (3S)-(9CI) is a complex organic compound characterized by its azepine ring structure, which is a seven-membered nitrogen-containing heterocycle. This compound features an acetic acid moiety and a fluorenylmethoxycarbonyl (Fmoc) protecting group, commonly used in peptide synthesis to protect amino groups. The presence of the hexahydro-2-oxo group indicates that it has a saturated cyclic structure with a ketone functionality, contributing to its reactivity and potential applications in medicinal chemistry. The stereochemistry at the 3-position of the azepine ring is specified as (3S), indicating a specific spatial arrangement of atoms that can influence the compound's biological activity and interactions. This compound may be of interest in pharmaceutical research due to its structural features, which could be relevant for the development of novel therapeutic agents. As with many organic compounds, its solubility, stability, and reactivity will depend on the specific conditions under which it is handled.

Formula: C₂₃H₂₄N₂O₅

(S)-2-(3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-oxoazepan-1-yl)acetic acid

CAS: 142855-79-6

Formula: C₂₃H₂₄N₂O₅

Purity: 95%

Color and Shape: Solid

Molecular weight: 408.4471

Ref: IN-DA007Z8Y

(S)-2-(3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-oxoazepan-1-yl)acetic acid

CAS: 142855-79-6

(S)-2-(3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-oxoazepan-1-yl)acetic acid

Purity: 95%

Molecular weight: 408.45g/mol

Ref: 54-OR1045038

(S)-2-(3-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-2-oxoazepan-1-yl)acetic acid

CAS: 142855-79-6

Purity: 95%

Molecular weight: 408.45401

Ref: 10-F769504

Fmoc-(3S)-3-amino-1-carboxymethylcaprolactame

Controlled Product

CAS: 142855-79-6

Applications Fmoc-(3S)-3-amino-1-carboxymethylcaprolactame is used in the synthesis of unsubstituted piperazinone-based transition state factor Xa inhibitors. It is also used to prepare peptidomimetics containing Freidinger lactams as STAT3 inhibitors.
References Huang, W., et al.: Bioorg. Med. Chem. Lett., 13, 723 (2003); Gomez, C., et al.: Bioog. Med. Chem. Lett., 19, 1733 (2009)

Formula: C₂₃H₂₄N₂O₅

Color and Shape: Neat

Molecular weight: 408.45

Ref: TR-F619985