1-Boc-2-(4-tetrahydropyranyl)hydrazine

97%

Reagent Code: #173402
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CAS Number 693287-79-5

science Other reagents with same CAS 693287-79-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 216.28 g/mol
Formula C₁₀H₂₀N₂O₃
badge Registry Numbers
MDL Number MFCD11044978
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a protected hydrazine building block in organic synthesis, particularly in pharmaceutical and agrochemical research. The Boc (tert-butoxycarbonyl) and THP (tetrahydropyranyl) groups act as orthogonal protecting groups for the hydrazine functionality, allowing selective deprotection and stepwise construction of complex molecules. It is especially valuable in the synthesis of hydrazide-containing compounds, heterocycles, and peptidomimetics where controlled reactivity is required. Its stability under various reaction conditions makes it suitable for multi-step synthetic routes.

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Test Parameter Specification
Appearance solid
Purity (%) 96.5-100%
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿638.00
inventory 1g
10-20 days ฿1,160.50
inventory 5g
10-20 days ฿10,030.00
inventory 25g
10-20 days ฿34,530.00

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1-Boc-2-(4-tetrahydropyranyl)hydrazine
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Used as a protected hydrazine building block in organic synthesis, particularly in pharmaceutical and agrochemical research. The Boc (tert-butoxycarbonyl) and THP (tetrahydropyranyl) groups act as orthogonal protecting groups for the hydrazine functionality, allowing selective deprotection and stepwise construction of complex molecules. It is especially valuable in the synthesis of hydrazide-containing compounds, heterocycles, and peptidomimetics where controlled reactivity is required. Its stability und

Used as a protected hydrazine building block in organic synthesis, particularly in pharmaceutical and agrochemical research. The Boc (tert-butoxycarbonyl) and THP (tetrahydropyranyl) groups act as orthogonal protecting groups for the hydrazine functionality, allowing selective deprotection and stepwise construction of complex molecules. It is especially valuable in the synthesis of hydrazide-containing compounds, heterocycles, and peptidomimetics where controlled reactivity is required. Its stability under various reaction conditions makes it suitable for multi-step synthetic routes.

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