N,N-Diisobutylnitrous amide

95%

Reagent Code: #219314
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CAS Number 997-95-5

science Other reagents with same CAS 997-95-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 158.24 g/mol
Formula C₈H₁₈N₂O
badge Registry Numbers
MDL Number MFCD00210333
inventory_2 Storage & Handling
Density 0.92±0.1 g/cm3
Storage -20°C, Inert Gas

description Product Description

Used primarily as a specialty reagent in organic synthesis, this compound serves as a nitrating agent and nitrosation source in the preparation of nitrogen-containing compounds. It enables the introduction of nitroso groups into active methylene compounds and secondary amines, facilitating the formation of oximes, nitrosamines, and heterocyclic structures. Its selective reactivity under mild conditions makes it valuable in pharmaceutical research for modifying complex molecules, particularly in the development of bioactive intermediates. Due to its sensitivity, it is typically handled in controlled environments and used in situ where possible.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿5,490.00
inventory 100mg
10-20 days ฿11,720.00
inventory 250mg
10-20 days ฿23,090.00
inventory 1g
10-20 days ฿65,500.00
inventory 5g
10-20 days ฿187,500.00
N,N-Diisobutylnitrous amide
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Used primarily as a specialty reagent in organic synthesis, this compound serves as a nitrating agent and nitrosation source in the preparation of nitrogen-containing compounds. It enables the introduction of nitroso groups into active methylene compounds and secondary amines, facilitating the formation of oximes, nitrosamines, and heterocyclic structures. Its selective reactivity under mild conditions makes it valuable in pharmaceutical research for modifying complex molecules, particularly in the devel

Used primarily as a specialty reagent in organic synthesis, this compound serves as a nitrating agent and nitrosation source in the preparation of nitrogen-containing compounds. It enables the introduction of nitroso groups into active methylene compounds and secondary amines, facilitating the formation of oximes, nitrosamines, and heterocyclic structures. Its selective reactivity under mild conditions makes it valuable in pharmaceutical research for modifying complex molecules, particularly in the development of bioactive intermediates. Due to its sensitivity, it is typically handled in controlled environments and used in situ where possible.

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