4-[3-(Trifluoromethyl)-3H-diazirin-3-yl]benzoic Acid

≥98%

Reagent Code: #118790
fingerprint
CAS Number 85559-46-2

science Other reagents with same CAS 85559-46-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 230.15 g/mol
Formula C₉H₅F₃N₂O₂
badge Registry Numbers
MDL Number MFCD00236809
thermostat Physical Properties
Melting Point 125°C(lit.)
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is widely used in photoaffinity labeling studies, a technique employed to investigate molecular interactions within biological systems. Its diazirine group, when exposed to ultraviolet light, generates a highly reactive carbene intermediate that can form covalent bonds with nearby molecules. This property makes it invaluable for mapping protein-ligand interactions, identifying binding sites, and studying protein-protein interactions. Additionally, it is utilized in the development of probes for studying enzyme mechanisms and receptor-ligand dynamics. Its trifluoromethyl group enhances its stability and reactivity, making it a preferred choice in biochemical research and drug discovery processes.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance White To Light Pink Solid
Purity (%) 98-100%
Proton NMR Spectrum Conforms to Structure
Infrared Spectrum Conforms To Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿20,600.00
inventory 200mg
10-20 days ฿6,650.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
4-[3-(Trifluoromethyl)-3H-diazirin-3-yl]benzoic Acid
No image available
This chemical is widely used in photoaffinity labeling studies, a technique employed to investigate molecular interactions within biological systems. Its diazirine group, when exposed to ultraviolet light, generates a highly reactive carbene intermediate that can form covalent bonds with nearby molecules. This property makes it invaluable for mapping protein-ligand interactions, identifying binding sites, and studying protein-protein interactions. Additionally, it is utilized in the development of probes for studying enzyme mechanisms and receptor-ligand dynamics. Its trifluoromethyl group enhances its stability and reactivity, making it a preferred choice in biochemical research and drug discovery processes.
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...