N-Boc-2-Aminothiazole

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Reagent Code: #217484
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CAS Number 170961-15-6

science Other reagents with same CAS 170961-15-6

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Weight 200.26 g/mol
Formula C₈H₁₂N₂O₂S
inventory_2 Storage & Handling
Storage  2-8°C

description Product Description

Widely used in pharmaceutical synthesis, this compound serves as a protected intermediate in the development of biologically active molecules. Its thiazole ring is commonly found in drugs with antimicrobial, antiviral, and anti-inflammatory properties. The Boc (tert-butoxycarbonyl) group provides temporary protection of the amine functionality, allowing selective reactions at other sites during multi-step syntheses. It is particularly valuable in the preparation of protease inhibitors and kinase inhibitors, where controlled deprotection and coupling steps are essential. Additionally, it supports solid-phase and solution-phase peptide-like assembly when thiazole-containing scaffolds are required. Its stability under various reaction conditions makes it suitable for use in combinatorial chemistry and high-throughput screening campaigns.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿280.00
inventory 5g
10-20 days ฿440.00

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N-Boc-2-Aminothiazole
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Widely used in pharmaceutical synthesis, this compound serves as a protected intermediate in the development of biologically active molecules. Its thiazole ring is commonly found in drugs with antimicrobial, antiviral, and anti-inflammatory properties. The Boc (tert-butoxycarbonyl) group provides temporary protection of the amine functionality, allowing selective reactions at other sites during multi-step syntheses. It is particularly valuable in the preparation of protease inhibitors and kinase inhibito

Widely used in pharmaceutical synthesis, this compound serves as a protected intermediate in the development of biologically active molecules. Its thiazole ring is commonly found in drugs with antimicrobial, antiviral, and anti-inflammatory properties. The Boc (tert-butoxycarbonyl) group provides temporary protection of the amine functionality, allowing selective reactions at other sites during multi-step syntheses. It is particularly valuable in the preparation of protease inhibitors and kinase inhibitors, where controlled deprotection and coupling steps are essential. Additionally, it supports solid-phase and solution-phase peptide-like assembly when thiazole-containing scaffolds are required. Its stability under various reaction conditions makes it suitable for use in combinatorial chemistry and high-throughput screening campaigns.

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