1217452-48-6

1217452-48-6 - Names and Identifiers

Name	N-(9-Fluorenylmethoxycarbonyl)-L-proline-13C5,15N, L-Proline-13C5,15N, N-Fmoc derivative
Synonyms	Fmoc-Pro-OH-13C5,15N [U-13C5,15N]-Fmoc-Pro-OH N-(9-Fluorenylmethoxycarbonyl)-L-proline-13C5,15N, L-Proline-13C5,15N, N-Fmoc derivative N-(9-Fluorenylmethoxycarbonyl)-L-proline-13C5,15N, L-Proline-13C5,15N, N-Fmoc derivative
CAS	1217452-48-6

1217452-48-6 - Physico-chemical Properties

Molecular Formula	C20H19NO4
Molar Mass	343.42316
Melting Point	117-118°C(lit.)
Storage Condition	2-8℃

1217452-48-6 - Risk and Safety

Hazard Symbols	Xi - Irritant
Risk Codes	36/37/38 - Irritating to eyes, respiratory system and skin.
Safety Description	S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36 - Wear suitable protective clothing.

1217452-48-6 - Introduction

N-(fluoromethoxycarbonyl)-L-proline-13C5,15N, L-Proline-13C5,15N, N-Fmoc derivative(N-(9-fluoromethoxycarbonyl)-L-proline-13C5,15N, L-proline-13C5,15N, N-Fmoc derivative) is an amino acid derivative with the following properties:

1. Appearance: White or off-white crystalline solid.
2. Molecular formula: C41H30FN4O6.
3. Molecular weight: 700.70g/mol.

This compound is mainly used for peptide synthesis and solid phase synthesis in Bioorganic Chemistry Research. It can be used as a protecting group for peptide synthesis, helping to protect the reactivity of amino acid functional groups for use in the selective synthesis of more complex peptide and protein structures.

The method for preparing this compound is usually to react 13C and 15N stable isotopes with N-protected proline (L-Proline) and 9-fluoromethoxycarbonyl (N-Fmoc) chemical coupling was performed.

Last Update：2024-04-10 22:29:15