(9H-Fluoren-9-yl) methyl carbonochloridate PurReagent, >=98%

PurReagent


Properties

Assay Purity >=98%
M pt. 62 - 64 °C
Form Solid

Safety Information

Hazard Statement(s) H314
Precautionary Statement  P260 - P280 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338 - P363
GHS Pictogram
Signal word Danger
HS Code NA
Storage Temp. 2-8°C
Storage Class 8A - Combustible corrosive hazardous materials
UN Number 3261

Description

Application
Widely used in peptide synthesis. Protects amine (-NH2) groups during stepwise reactions. Important in solid-phase peptide synthesis (SPPS). Used in preparation of amino acid derivatives.

Purpose
Acts as a protecting reagent for amines. Allows selective reactions by temporarily blocking reactive groups. Helps in building complex biomolecules like peptides in a controlled manner.

General Description
Reactive organic compound derived from fluorene. Contains a chloroformate (-OCOCl) functional group. Typically a solid moisture-sensitive and used under controlled conditions. Commonly known as Fmoc-Cl a key reagent in organic synthesis.