2-cycloheptylidene-, 1,1-dimethylethyl ester Hydrazinecarboxylic acid

98%

Reagent Code: #245665
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CAS Number 79201-40-4

science Other reagents with same CAS 79201-40-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 226.32 g/mol
Formula C₁₂H₂₂N₂O₂
thermostat Physical Properties
Melting Point 122-123 °C
inventory_2 Storage & Handling
Density 1.06±0.1 g/cm3(Predicted)
Storage -20°C, Sealed, Dry

description Product Description

Used primarily as a specialty reagent in organic synthesis, particularly in the preparation of hydrazide derivatives and heterocyclic compounds. It serves as a protecting group for hydrazine in peptide and nucleotide synthesis due to its stability under various reaction conditions. The compound is also employed in the development of pharmaceutical intermediates where controlled release of hydrazine is required. Its bulky tert-butyl group enhances selectivity in condensation reactions, making it valuable in fine chemical manufacturing. Additionally, it finds use in polymer chemistry as a cross-linking agent or initiator in certain curing processes.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿5,930.00
inventory 25mg
10-20 days ฿18,690.00
inventory 10mg
10-20 days ฿9,450.00

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2-cycloheptylidene-, 1,1-dimethylethyl ester Hydrazinecarboxylic acid
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Used primarily as a specialty reagent in organic synthesis, particularly in the preparation of hydrazide derivatives and heterocyclic compounds. It serves as a protecting group for hydrazine in peptide and nucleotide synthesis due to its stability under various reaction conditions. The compound is also employed in the development of pharmaceutical intermediates where controlled release of hydrazine is required. Its bulky tert-butyl group enhances selectivity in condensation reactions, making it valuable

Used primarily as a specialty reagent in organic synthesis, particularly in the preparation of hydrazide derivatives and heterocyclic compounds. It serves as a protecting group for hydrazine in peptide and nucleotide synthesis due to its stability under various reaction conditions. The compound is also employed in the development of pharmaceutical intermediates where controlled release of hydrazine is required. Its bulky tert-butyl group enhances selectivity in condensation reactions, making it valuable in fine chemical manufacturing. Additionally, it finds use in polymer chemistry as a cross-linking agent or initiator in certain curing processes.

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