Tert-butyl 2-ethylhydrazinecarboxylate

≥95%

Reagent Code: #240225
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CAS Number 476362-41-1

science Other reagents with same CAS 476362-41-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 160.21 g/mol
Formula C₇H₁₆N₂O₂
badge Registry Numbers
MDL Number MFCD22380479
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a hydrazine protecting group in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its protected hydrazine functionality allows selective reactions in multi-step syntheses, improving yield and reducing side reactions. Commonly employed in the formation of heterocyclic compounds such as pyrazoles and triazoles, which are key motifs in drug discovery. Also utilized in peptide modification and bioconjugation due to its stability under various reaction conditions and clean deprotection profile.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿6,270.00
inventory 1g
10-20 days ฿16,420.00
inventory 5g
10-20 days ฿66,830.00
Tert-butyl 2-ethylhydrazinecarboxylate
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Used as a hydrazine protecting group in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its protected hydrazine functionality allows selective reactions in multi-step syntheses, improving yield and reducing side reactions. Commonly employed in the formation of heterocyclic compounds such as pyrazoles and triazoles, which are key motifs in drug discovery. Also utilized in peptide modification and bioconjugation due to its stability under various reaction conditions

Used as a hydrazine protecting group in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its protected hydrazine functionality allows selective reactions in multi-step syntheses, improving yield and reducing side reactions. Commonly employed in the formation of heterocyclic compounds such as pyrazoles and triazoles, which are key motifs in drug discovery. Also utilized in peptide modification and bioconjugation due to its stability under various reaction conditions and clean deprotection profile.

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