N-BOC-IMINO-(TRIPHENYL)PHOSPHORANE

98%

Reagent Code: #60093
label
Alias N-tert-butoxycarbonylimine(triphenyl)phosphineN-BOC-iminotriphenylphosphineN-BOC-iminotriphenylphosphinetriphenylphosphinoiminocarbamate tert-butyl esterN-BOC- Triphenylphosphorimide N-BOC-triphenylphosphorimide
fingerprint
CAS Number 68014-21-1

science Other reagents with same CAS 68014-21-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 377.42 g/mol
Formula C₂₃H₂₄NO₂P
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This chemical is primarily used in organic synthesis, particularly in the preparation of protected amino acids and peptides. It serves as a key reagent in the formation of imines and other nitrogen-containing compounds, facilitating the introduction of the BOC (tert-butoxycarbonyl) protecting group. This protecting group is crucial in peptide synthesis as it shields the amine functionality during reactions, allowing selective deprotection at a later stage. The compound is also employed in the synthesis of complex organic molecules, including pharmaceuticals and natural products, where precise control over nitrogen-based functional groups is required. Its stability and reactivity make it a valuable tool in the development of novel chemical entities and in the modification of biomolecules.

format_list_bulleted Product Specification

Test Parameter Specification
Purity 98-100%
Appearance White to light yellow powder
Proton NMR Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿520.00
inventory 1g
10-20 days ฿300.00
inventory 250mg
10-20 days ฿290.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
N-BOC-IMINO-(TRIPHENYL)PHOSPHORANE
No image available
This chemical is primarily used in organic synthesis, particularly in the preparation of protected amino acids and peptides. It serves as a key reagent in the formation of imines and other nitrogen-containing compounds, facilitating the introduction of the BOC (tert-butoxycarbonyl) protecting group. This protecting group is crucial in peptide synthesis as it shields the amine functionality during reactions, allowing selective deprotection at a later stage. The compound is also employed in the synthesis of complex organic molecules, including pharmaceuticals and natural products, where precise control over nitrogen-based functional groups is required. Its stability and reactivity make it a valuable tool in the development of novel chemical entities and in the modification of biomolecules.
Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...