N-(Tert-butoxycarbonylamino)phthalimide

95%

Reagent Code: #80161
fingerprint
CAS Number 34387-89-8

science Other reagents with same CAS 34387-89-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 262.26 g/mol
Formula C₁₃H₁₄N₂O₄
badge Registry Numbers
MDL Number MFCD00686624
inventory_2 Storage & Handling
Storage Room temperature, dry, sealed

description Product Description

This compound is primarily used in organic synthesis as a protecting group for amines. It is particularly effective in peptide synthesis, where it safeguards the amino group during reactions involving other functional groups. The tert-butoxycarbonyl (Boc) group can be easily removed under acidic conditions, allowing for the controlled deprotection of the amine when needed. Additionally, it finds application in the preparation of pharmaceuticals and agrochemicals, where selective protection of amines is crucial for the synthesis of complex molecules. Its stability under basic conditions and compatibility with various reaction conditions make it a versatile reagent in synthetic chemistry.

format_list_bulleted Product Specification

Test Parameter Specification
APPEARANCE White to off-white to light yellow Solid
Purity (%) 94.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿693.00
inventory 5g
10-20 days ฿2,493.00
inventory 25g
10-20 days ฿8,739.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
N-(Tert-butoxycarbonylamino)phthalimide
No image available
This compound is primarily used in organic synthesis as a protecting group for amines. It is particularly effective in peptide synthesis, where it safeguards the amino group during reactions involving other functional groups. The tert-butoxycarbonyl (Boc) group can be easily removed under acidic conditions, allowing for the controlled deprotection of the amine when needed. Additionally, it finds application in the preparation of pharmaceuticals and agrochemicals, where selective protection of amines is cruc
This compound is primarily used in organic synthesis as a protecting group for amines. It is particularly effective in peptide synthesis, where it safeguards the amino group during reactions involving other functional groups. The tert-butoxycarbonyl (Boc) group can be easily removed under acidic conditions, allowing for the controlled deprotection of the amine when needed. Additionally, it finds application in the preparation of pharmaceuticals and agrochemicals, where selective protection of amines is crucial for the synthesis of complex molecules. Its stability under basic conditions and compatibility with various reaction conditions make it a versatile reagent in synthetic chemistry.
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...