tert-butyl (2-(4-chloro-3-fluorophenyl)-2-hydroxyethyl)carbamate
- Product Code: 54848
CAS:
1445669-99-7
| Molecular Weight: | 289.73 g./mol | Molecular Formula: | C₁₃H₁₇ClFNO₃ |
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| Density: | Storage Condition: | 2-8℃ |
Product Description:
This chemical is primarily used in the pharmaceutical and agrochemical industries as an intermediate in the synthesis of more complex molecules. Its structure, featuring both a carbamate group and a hydroxyl group, makes it valuable for constructing active pharmaceutical ingredients (APIs) or agrochemical compounds.
In pharmaceuticals, it can serve as a building block for drugs targeting specific biological pathways, particularly those involving enzyme inhibition or receptor modulation. The presence of the chloro and fluoro substituents on the phenyl ring enhances its potential for interactions with biological targets, making it useful in the development of compounds with antimicrobial, antifungal, or anti-inflammatory properties.
In agrochemicals, it may be utilized to create pesticides or herbicides, where the halogenated aromatic ring contributes to the compound's ability to disrupt pest or weed growth. The tert-butyl group provides steric bulk, which can be advantageous in optimizing the efficacy and stability of the final product.
Overall, its versatile structure allows for modifications that tailor its application to specific industrial or research needs.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.200 | 10-20 days | $353.93 |
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tert-butyl (2-(4-chloro-3-fluorophenyl)-2-hydroxyethyl)carbamate
This chemical is primarily used in the pharmaceutical and agrochemical industries as an intermediate in the synthesis of more complex molecules. Its structure, featuring both a carbamate group and a hydroxyl group, makes it valuable for constructing active pharmaceutical ingredients (APIs) or agrochemical compounds.
In pharmaceuticals, it can serve as a building block for drugs targeting specific biological pathways, particularly those involving enzyme inhibition or receptor modulation. The presence of the chloro and fluoro substituents on the phenyl ring enhances its potential for interactions with biological targets, making it useful in the development of compounds with antimicrobial, antifungal, or anti-inflammatory properties.
In agrochemicals, it may be utilized to create pesticides or herbicides, where the halogenated aromatic ring contributes to the compound's ability to disrupt pest or weed growth. The tert-butyl group provides steric bulk, which can be advantageous in optimizing the efficacy and stability of the final product.
Overall, its versatile structure allows for modifications that tailor its application to specific industrial or research needs.
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