1-(1-Trityl-1H-imidazol-4-yl)ethanone

95%

Reagent Code: #39099
fingerprint
CAS Number 116795-55-2

science Other reagents with same CAS 116795-55-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 352.4400 g/mol
Formula C₂₄H₂₀N₂O
badge Registry Numbers
MDL Number MFCD17215519
inventory_2 Storage & Handling
Storage room temperature

description Product Description

Used primarily in organic synthesis, this compound serves as a key intermediate in the preparation of more complex molecules, particularly in pharmaceutical research. It is often employed in the development of imidazole-based compounds, which are known for their biological activity. The trityl group provides stability and protection during chemical reactions, making it valuable in multi-step synthetic processes. Its application extends to the study of enzyme inhibition and receptor binding, aiding in the discovery of new therapeutic agents. Additionally, it is utilized in material science for the design of functionalized polymers and coatings.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance White Solid
Purity (%) 94.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,376.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
1-(1-Trityl-1H-imidazol-4-yl)ethanone
No image available

Used primarily in organic synthesis, this compound serves as a key intermediate in the preparation of more complex molecules, particularly in pharmaceutical research. It is often employed in the development of imidazole-based compounds, which are known for their biological activity. The trityl group provides stability and protection during chemical reactions, making it valuable in multi-step synthetic processes. Its application extends to the study of enzyme inhibition and receptor binding, aiding in the

Used primarily in organic synthesis, this compound serves as a key intermediate in the preparation of more complex molecules, particularly in pharmaceutical research. It is often employed in the development of imidazole-based compounds, which are known for their biological activity. The trityl group provides stability and protection during chemical reactions, making it valuable in multi-step synthetic processes. Its application extends to the study of enzyme inhibition and receptor binding, aiding in the discovery of new therapeutic agents. Additionally, it is utilized in material science for the design of functionalized polymers and coatings.

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...