2-Nitrobenzyl bromide
97%
- Product Code: 116980
Alias:
2-nitrobenzyl bromide; o-nitrobenzyl bromide
CAS:
3958-60-9
| Molecular Weight: | 216.03 g./mol | Molecular Formula: | C₇H₆BrNO₂ |
|---|---|---|---|
| EC Number: | 223-558-9 | MDL Number: | MFCD00007184 |
| Melting Point: | 44-46 °C(lit.) | Boiling Point: | |
| Density: | Storage Condition: | 2~8°C |
Product Description:
Used primarily in organic synthesis as a photolabile protecting group for carboxylic acids, alcohols, and amines. It is particularly valuable in the development of photoresponsive materials and controlled-release systems, where light-induced deprotection is required. In peptide chemistry, it serves as a temporary protecting group that can be removed under mild conditions using UV light, minimizing damage to sensitive structures. Additionally, it finds applications in the preparation of photoactivatable probes and caged compounds for biochemical studies, enabling precise spatial and temporal control over the release of active molecules.
Product Specification:
| Test | Specification |
|---|---|
| Melting Point | 45-48 |
| Purity (GC) | 97-100% |
| Appearance | Yellow To Tan Powder |
| Infrared Spectrum | Conforms To Structure |
| Note | Low Melting Point Solid |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 | 10-20 days | ฿350.00 |
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| 25.000 | 10-20 days | ฿1,500.00 |
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| 100.000 | 10-20 days | ฿5,900.00 |
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| 500.000 | 10-20 days | ฿29,370.00 |
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2-Nitrobenzyl bromide
Used primarily in organic synthesis as a photolabile protecting group for carboxylic acids, alcohols, and amines. It is particularly valuable in the development of photoresponsive materials and controlled-release systems, where light-induced deprotection is required. In peptide chemistry, it serves as a temporary protecting group that can be removed under mild conditions using UV light, minimizing damage to sensitive structures. Additionally, it finds applications in the preparation of photoactivatable probes and caged compounds for biochemical studies, enabling precise spatial and temporal control over the release of active molecules.
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