tert-Butyl 2-(tert-butyl)hydrazinecarboxylate

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Reagent Code: #115876
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CAS Number 60295-52-5

science Other reagents with same CAS 60295-52-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 188.27 g/mol
Formula C₉H₂₀N₂O₂
badge Registry Numbers
MDL Number MFCD04125557
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

This chemical is primarily utilized in organic synthesis as a protecting group for hydrazines. It helps stabilize hydrazine derivatives during complex reactions, preventing unwanted side reactions. It is also employed in the preparation of pharmaceuticals and agrochemicals, where controlled release or selective reactivity of hydrazine intermediates is required. Additionally, it serves as a building block in the synthesis of heterocyclic compounds, which are crucial in drug discovery and development. Its tert-butyl groups provide steric protection, enhancing the selectivity of chemical transformations.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿1,908.00
inventory 1g
10-20 days ฿486.00
inventory 10g
10-20 days ฿3,222.00

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tert-Butyl 2-(tert-butyl)hydrazinecarboxylate
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This chemical is primarily utilized in organic synthesis as a protecting group for hydrazines. It helps stabilize hydrazine derivatives during complex reactions, preventing unwanted side reactions. It is also employed in the preparation of pharmaceuticals and agrochemicals, where controlled release or selective reactivity of hydrazine intermediates is required. Additionally, it serves as a building block in the synthesis of heterocyclic compounds, which are crucial in drug discovery and development. Its ter
This chemical is primarily utilized in organic synthesis as a protecting group for hydrazines. It helps stabilize hydrazine derivatives during complex reactions, preventing unwanted side reactions. It is also employed in the preparation of pharmaceuticals and agrochemicals, where controlled release or selective reactivity of hydrazine intermediates is required. Additionally, it serves as a building block in the synthesis of heterocyclic compounds, which are crucial in drug discovery and development. Its tert-butyl groups provide steric protection, enhancing the selectivity of chemical transformations.
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