4-[3-(Trifluoromethyl)-3H-diaziridine]benzyl Alcohol tert-Butyl(dimethyl)silyl Ether
95%
- Product Code: 86109
CAS:
87736-83-2
| Molecular Weight: | 332.44 g./mol | Molecular Formula: | C₁₅H₂₃F₃N₂OSi |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 325.5±52.0 °C(Predicted) | |
| Density: | 1.113±0.06 g/cm3(Predicted) | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily utilized in the field of organic synthesis and biochemistry as a photoactivatable crosslinking agent. Its diazirine group allows it to form covalent bonds with nearby molecules upon exposure to ultraviolet light, making it valuable for studying protein-protein interactions, ligand-receptor binding, and other molecular interactions. The tert-butyldimethylsilyl (TBDMS) ether group serves as a protective moiety for the hydroxyl group, ensuring stability during synthetic processes. This compound is particularly useful in proteomics and molecular biology research, where it aids in mapping interaction sites and elucidating complex biological pathways. Its trifluoromethyl group enhances its reactivity and selectivity, making it a versatile tool in chemical biology and drug discovery.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿99,000.00 |
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4-[3-(Trifluoromethyl)-3H-diaziridine]benzyl Alcohol tert-Butyl(dimethyl)silyl Ether
This chemical is primarily utilized in the field of organic synthesis and biochemistry as a photoactivatable crosslinking agent. Its diazirine group allows it to form covalent bonds with nearby molecules upon exposure to ultraviolet light, making it valuable for studying protein-protein interactions, ligand-receptor binding, and other molecular interactions. The tert-butyldimethylsilyl (TBDMS) ether group serves as a protective moiety for the hydroxyl group, ensuring stability during synthetic processes. This compound is particularly useful in proteomics and molecular biology research, where it aids in mapping interaction sites and elucidating complex biological pathways. Its trifluoromethyl group enhances its reactivity and selectivity, making it a versatile tool in chemical biology and drug discovery.
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