2-Hydroxy-4-(3-(trifluoromethyl)-3H-diazirin-3-yl)benzaldehyde
97%
- Product Code: 197998
CAS:
308085-25-8
| Molecular Weight: | 230.14 g./mol | Molecular Formula: | C₉H₅F₃N₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD30468740 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
Used primarily as a photoactivatable crosslinking agent in biochemical and proteomic research. Its key application lies in labeling and capturing transient protein-protein or protein-ligand interactions. Upon exposure to UV light, the diazirine group generates highly reactive carbenes that insert nonspecifically into nearby C-H, N-H, or O-H bonds, forming covalent links between interacting biomolecules. The aldehyde and hydroxyl functional groups allow further chemical modification, such as conjugation to probes or solid supports. This makes it valuable for studying molecular interactions in complex biological systems, including membrane receptors, enzyme-substrate complexes, and signaling pathways.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | ฿47,190.00 |
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| 250mg | 10-20 days | ฿78,290.00 |
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2-Hydroxy-4-(3-(trifluoromethyl)-3H-diazirin-3-yl)benzaldehyde
Used primarily as a photoactivatable crosslinking agent in biochemical and proteomic research. Its key application lies in labeling and capturing transient protein-protein or protein-ligand interactions. Upon exposure to UV light, the diazirine group generates highly reactive carbenes that insert nonspecifically into nearby C-H, N-H, or O-H bonds, forming covalent links between interacting biomolecules. The aldehyde and hydroxyl functional groups allow further chemical modification, such as conjugation to probes or solid supports. This makes it valuable for studying molecular interactions in complex biological systems, including membrane receptors, enzyme-substrate complexes, and signaling pathways.
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