3-Nitro-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrazole

95%

Reagent Code: #124212
fingerprint
CAS Number 1313520-83-0

science Other reagents with same CAS 1313520-83-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 243.34 g/mol
Formula C₉H₁₇N₃O₃Si
badge Registry Numbers
MDL Number MFCD28128954
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used in organic synthesis as a protected intermediate for pyrazole derivatives, particularly in the development of pharmaceuticals and agrochemicals. The trimethylsilyl ethoxymethyl (SEM) group acts as a protective group for the nitrogen atom, allowing selective reactions at other sites of the molecule. It is also employed in the preparation of complex heterocyclic compounds, where the nitro group can be reduced or further functionalized. This compound is valuable in medicinal chemistry for creating drug candidates with specific biological activities.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,360.00
inventory 250mg
10-20 days ฿17,262.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
3-Nitro-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrazole
No image available

Used in organic synthesis as a protected intermediate for pyrazole derivatives, particularly in the development of pharmaceuticals and agrochemicals. The trimethylsilyl ethoxymethyl (SEM) group acts as a protective group for the nitrogen atom, allowing selective reactions at other sites of the molecule. It is also employed in the preparation of complex heterocyclic compounds, where the nitro group can be reduced or further functionalized. This compound is valuable in medicinal chemistry for creating drug

Used in organic synthesis as a protected intermediate for pyrazole derivatives, particularly in the development of pharmaceuticals and agrochemicals. The trimethylsilyl ethoxymethyl (SEM) group acts as a protective group for the nitrogen atom, allowing selective reactions at other sites of the molecule. It is also employed in the preparation of complex heterocyclic compounds, where the nitro group can be reduced or further functionalized. This compound is valuable in medicinal chemistry for creating drug candidates with specific biological activities.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...