Tert-Butyl 2-(2-Chlorobenzyl)Hydrazinecarboxylate
95%
- Product Code: 84431
CAS:
135941-95-6
| Molecular Weight: | 256.73 g./mol | Molecular Formula: | C₁₂H₁₇ClN₂O₂ |
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| EC Number: | MDL Number: | MFCD24873145 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in organic synthesis as a versatile intermediate for the preparation of various pharmacologically active molecules. It serves as a key building block in the development of hydrazine derivatives, which are often explored for their potential therapeutic applications, particularly in the synthesis of anticancer and antimicrobial agents. The tert-butyl group provides stability and facilitates selective reactions, while the chlorobenzyl moiety can be further modified to introduce specific functional groups, enhancing the compound's reactivity and utility in complex synthetic pathways. Its application extends to the field of medicinal chemistry, where it is employed in the design and synthesis of novel drug candidates targeting specific biological pathways.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿9,360.00 |
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| 0.250 | 10-20 days | ฿16,380.00 |
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| 1.000 | 10-20 days | ฿32,760.00 |
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Tert-Butyl 2-(2-Chlorobenzyl)Hydrazinecarboxylate
This compound is primarily utilized in organic synthesis as a versatile intermediate for the preparation of various pharmacologically active molecules. It serves as a key building block in the development of hydrazine derivatives, which are often explored for their potential therapeutic applications, particularly in the synthesis of anticancer and antimicrobial agents. The tert-butyl group provides stability and facilitates selective reactions, while the chlorobenzyl moiety can be further modified to introduce specific functional groups, enhancing the compound's reactivity and utility in complex synthetic pathways. Its application extends to the field of medicinal chemistry, where it is employed in the design and synthesis of novel drug candidates targeting specific biological pathways.
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