1,1,2-Tris(tert-butoxycarbonyl)hydrazine

95%

Reagent Code: #242913
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CAS Number 185456-26-2

science Other reagents with same CAS 185456-26-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 332.39 g/mol
Formula C₁₅H₂₈N₂O₆
badge Registry Numbers
MDL Number MFCD04973130
thermostat Physical Properties
Melting Point 109-110 °C
inventory_2 Storage & Handling
Density 1.097±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used as a protecting group reagent in peptide synthesis and organic chemistry, particularly for selective protection of hydrazine derivatives. Its main application lies in the synthesis of complex molecules where controlled deprotection is required, such as in the preparation of pharmaceutical intermediates and bioactive compounds. The tert-butoxycarbonyl (Boc) groups allow for stepwise deprotection under mild acidic conditions, enabling precise manipulation of functional groups in multi-step syntheses. It is especially valuable in the construction of nitrogen-containing heterocycles and in the development of protease inhibitors.

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Size Availability Unit Price Quantity
inventory 10g
10-20 days ฿5,120.00
inventory 5g
10-20 days ฿2,580.00

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1,1,2-Tris(tert-butoxycarbonyl)hydrazine
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Used as a protecting group reagent in peptide synthesis and organic chemistry, particularly for selective protection of hydrazine derivatives. Its main application lies in the synthesis of complex molecules where controlled deprotection is required, such as in the preparation of pharmaceutical intermediates and bioactive compounds. The tert-butoxycarbonyl (Boc) groups allow for stepwise deprotection under mild acidic conditions, enabling precise manipulation of functional groups in multi-step syntheses.

Used as a protecting group reagent in peptide synthesis and organic chemistry, particularly for selective protection of hydrazine derivatives. Its main application lies in the synthesis of complex molecules where controlled deprotection is required, such as in the preparation of pharmaceutical intermediates and bioactive compounds. The tert-butoxycarbonyl (Boc) groups allow for stepwise deprotection under mild acidic conditions, enabling precise manipulation of functional groups in multi-step syntheses. It is especially valuable in the construction of nitrogen-containing heterocycles and in the development of protease inhibitors.

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