Tert-Butyl (2-methylthiazol-4-yl)carbamate

97%

Reagent Code: #238226
fingerprint
CAS Number 848472-61-7

science Other reagents with same CAS 848472-61-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 214.2847 g/mol
Formula C₉H₁₄N₂O₂S
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as an intermediate in pharmaceutical synthesis, particularly in the development of kinase inhibitors and antimicrobial agents. The thiazole ring combined with the tert-butoxycarbonyl (Boc) protecting group makes it valuable in peptide and heterocyclic chemistry, where selective protection of amino groups is required. It serves as a building block in the preparation of bioactive molecules, including those with antitumor and anti-inflammatory properties. Its stability under various reaction conditions allows for use in multi-step organic syntheses, especially in medicinal chemistry research and drug discovery.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,340.00
inventory 250mg
10-20 days ฿10,560.00
inventory 1g
10-20 days ฿26,360.00
inventory 5g
10-20 days ฿70,900.00
Tert-Butyl (2-methylthiazol-4-yl)carbamate
No image available

Used as an intermediate in pharmaceutical synthesis, particularly in the development of kinase inhibitors and antimicrobial agents. The thiazole ring combined with the tert-butoxycarbonyl (Boc) protecting group makes it valuable in peptide and heterocyclic chemistry, where selective protection of amino groups is required. It serves as a building block in the preparation of bioactive molecules, including those with antitumor and anti-inflammatory properties. Its stability under various reaction conditions

Used as an intermediate in pharmaceutical synthesis, particularly in the development of kinase inhibitors and antimicrobial agents. The thiazole ring combined with the tert-butoxycarbonyl (Boc) protecting group makes it valuable in peptide and heterocyclic chemistry, where selective protection of amino groups is required. It serves as a building block in the preparation of bioactive molecules, including those with antitumor and anti-inflammatory properties. Its stability under various reaction conditions allows for use in multi-step organic syntheses, especially in medicinal chemistry research and drug discovery.

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...