tert-Butyl (1-bromo-2-methylpropan-2-yl)carbamate

95%

Reagent Code: #128172
fingerprint
CAS Number 1391026-60-0

science Other reagents with same CAS 1391026-60-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 252.15 g/mol
Formula C₉H₁₈BrNO₂
badge Registry Numbers
MDL Number MFCD24166837
inventory_2 Storage & Handling
Storage -20°C, Inert Gas

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It serves as a protected amine derivative, enabling selective reactions in multi-step syntheses. The tert-butyloxycarbonyl (Boc) group provides stability under various reaction conditions and can be removed under mild acidic conditions, making it valuable in peptide synthesis and medicinal chemistry. The bromo substituent allows for further functionalization via cross-coupling reactions or nucleophilic substitution, facilitating the construction of complex molecules.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance Off-White Powder
Purity (%) 94.5-100
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,200.00
inventory 250mg
10-20 days ฿11,520.00
inventory 500mg
10-20 days ฿19,200.00
inventory 1g
10-20 days ฿28,800.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
tert-Butyl (1-bromo-2-methylpropan-2-yl)carbamate
No image available
Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It serves as a protected amine derivative, enabling selective reactions in multi-step syntheses. The tert-butyloxycarbonyl (Boc) group provides stability under various reaction conditions and can be removed under mild acidic conditions, making it valuable in peptide synthesis and medicinal chemistry. The bromo substituent allows for further functionalization via cross-coupling reactions or nuc
Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It serves as a protected amine derivative, enabling selective reactions in multi-step syntheses. The tert-butyloxycarbonyl (Boc) group provides stability under various reaction conditions and can be removed under mild acidic conditions, making it valuable in peptide synthesis and medicinal chemistry. The bromo substituent allows for further functionalization via cross-coupling reactions or nucleophilic substitution, facilitating the construction of complex molecules.
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...