4-[3-(Trifluoromethyl)-3H-diazirin-3-yl]benzoic Acid
≥98%
- Product Code: 118790
CAS:
85559-46-2
| Molecular Weight: | 230.15 g./mol | Molecular Formula: | C₉H₅F₃N₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00236809 | |
| Melting Point: | 125°C(lit.) | Boiling Point: | |
| Density: | Storage Condition: | 2-8°C |
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.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | White To Light Pink Solid |
| Purity (%) | 98-100 |
| Proton Nmr Spectrum | Conforms To Structure |
| Infrared Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.200 | 10-20 days | Ft71,647.82 |
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| 1.000 | 10-20 days | Ft221,946.62 |
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4-[3-(Trifluoromethyl)-3H-diazirin-3-yl]benzoic Acid
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.
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