Benzyl (3-bromopropyl)carbamate
97%
- Product Code: 118073
CAS:
39945-54-5
Molecular Weight: | 272.14 g./mol | Molecular Formula: | C₁₁H₁₄BrNO₂ |
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EC Number: | MDL Number: | MFCD01737871 | |
Melting Point: | Boiling Point: | 366.4°C at 760 mmHg | |
Density: | 1.377g/cm3 | Storage Condition: | -20°C, dry sealed |
Product Description:
Used primarily in organic synthesis as a versatile intermediate for constructing more complex molecules. It is particularly valuable in the development of pharmaceuticals, where it serves as a precursor for active compounds. The bromoalkyl group enables further functionalization through nucleophilic substitution reactions, making it useful in the creation of targeted drug molecules. Additionally, it finds application in the preparation of polymers and specialty chemicals, where its reactive sites allow for tailored modifications to achieve desired properties. Its role in peptide synthesis is also notable, as it can act as a protecting group for amines during multi-step reactions.
Product Specification:
Test | Specification |
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Appearance | White To Light Yellow To Yellow To Orange To Brown Solid |
Purity (%) | 96.5-100 |
Infrared Spectrum | Conforms To Structure |
NMR | Conforms To Structure |
Note | This Product Is Low Melting Point Solid, May Change State In Different Environments (Solid, Liquid Or Semi-Solid) |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.250 | 10-20 days | $54.31 |
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1.000 | 10-20 days | $135.91 |
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5.000 | 10-20 days | $525.65 |
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10.000 | 10-20 days | $823.88 |
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Benzyl (3-bromopropyl)carbamate
Used primarily in organic synthesis as a versatile intermediate for constructing more complex molecules. It is particularly valuable in the development of pharmaceuticals, where it serves as a precursor for active compounds. The bromoalkyl group enables further functionalization through nucleophilic substitution reactions, making it useful in the creation of targeted drug molecules. Additionally, it finds application in the preparation of polymers and specialty chemicals, where its reactive sites allow for tailored modifications to achieve desired properties. Its role in peptide synthesis is also notable, as it can act as a protecting group for amines during multi-step reactions.
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