2-(Boc-amino)-5-bromothiazole

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Reagent Code: #121413
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CAS Number 405939-39-1

science Other reagents with same CAS 405939-39-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 279.15 g/mol
Formula C₈H₁₁BrN₂O₂S
inventory_2 Storage & Handling
Storage room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs). It plays a role in the preparation of compounds with potential therapeutic applications, such as antiviral or anticancer agents. The Boc-protecting group ensures selective reactivity during chemical transformations, while the bromo substituent allows for further functionalization through cross-coupling reactions. This compound is valuable in medicinal chemistry for constructing complex molecules with specific biological activities.

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Test Parameter Specification
Purity (%) 97.5-100%
Infrared Spectrum Conforms To Structure
Proton NMR Spectrum Conforms to Structure
Appearance White to yellow to pale-brown solid

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿860.00
inventory 200mg
10-20 days ฿360.00
inventory 5g
10-20 days ฿3,520.00

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2-(Boc-amino)-5-bromothiazole
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs). It plays a role in the preparation of compounds with potential therapeutic applications, such as antiviral or anticancer agents. The Boc-protecting group ensures selective reactivity during chemical transformations, while the bromo substituent allows for further functionalization through cross-coupling reactions. This compound is valuable in medicinal chemistry for con

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs). It plays a role in the preparation of compounds with potential therapeutic applications, such as antiviral or anticancer agents. The Boc-protecting group ensures selective reactivity during chemical transformations, while the bromo substituent allows for further functionalization through cross-coupling reactions. This compound is valuable in medicinal chemistry for constructing complex molecules with specific biological activities.

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