4,5-Dimethoxy-2-nitrobenzyl carbonochloridate
≥95%
- Product Code: 45904
CAS:
42855-00-5
| Molecular Weight: | 275.64 g./mol | Molecular Formula: | C₁₀H₁₀ClNO₆ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00143507 | |
| Melting Point: | 125°C | Boiling Point: | 396.4°C at 760 mmHg |
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
Used primarily in organic synthesis, this compound serves as a protective group for alcohols and amines, enabling selective reactions in complex molecule construction. It is particularly valuable in peptide and carbohydrate chemistry, where temporary protection of functional groups is essential. Additionally, it finds application in photolabile protecting strategies, allowing controlled release of active molecules under light exposure, which is useful in drug delivery systems and photochemical studies. Its nitrobenzyl group facilitates cleavage upon UV irradiation, making it suitable for light-triggered applications in research and industrial processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | $27.00 |
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| 0.250 | 10-20 days | $42.66 |
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| 1.000 | 10-20 days | $122.59 |
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| 5.000 | 10-20 days | $431.50 |
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4,5-Dimethoxy-2-nitrobenzyl carbonochloridate
Used primarily in organic synthesis, this compound serves as a protective group for alcohols and amines, enabling selective reactions in complex molecule construction. It is particularly valuable in peptide and carbohydrate chemistry, where temporary protection of functional groups is essential. Additionally, it finds application in photolabile protecting strategies, allowing controlled release of active molecules under light exposure, which is useful in drug delivery systems and photochemical studies. Its nitrobenzyl group facilitates cleavage upon UV irradiation, making it suitable for light-triggered applications in research and industrial processes.
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