tert-Butyl (1-acetylcyclopropyl)carbamate
95%
- Product Code: 36129
CAS:
1159733-73-9
| Molecular Weight: | 199.25 g./mol | Molecular Formula: | C₁₀H₁₇NO₃ |
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| EC Number: | MDL Number: | MFCD24470943 | |
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| Density: | Storage Condition: | room temperature |
Product Description:
tert-Butyl (1-acetylcyclopropyl)carbamate is primarily used in organic synthesis as a versatile intermediate for the preparation of more complex chemical compounds. Its structure, featuring both a tert-butyl carbamate group and an acetylcyclopropyl moiety, makes it valuable in the development of pharmaceuticals, particularly in the synthesis of active pharmaceutical ingredients (APIs). The compound is often employed in medicinal chemistry for the construction of cyclopropane-containing molecules, which are known for their unique biological activities and stability. Additionally, it serves as a protective group for amines during multi-step synthetic processes, enabling selective reactions in the presence of sensitive functional groups. Its application extends to the field of agrochemicals, where it contributes to the synthesis of novel pesticides and herbicides with enhanced efficacy.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.025 | 10-20 days | ฿8,685.00 |
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tert-Butyl (1-acetylcyclopropyl)carbamate
tert-Butyl (1-acetylcyclopropyl)carbamate is primarily used in organic synthesis as a versatile intermediate for the preparation of more complex chemical compounds. Its structure, featuring both a tert-butyl carbamate group and an acetylcyclopropyl moiety, makes it valuable in the development of pharmaceuticals, particularly in the synthesis of active pharmaceutical ingredients (APIs). The compound is often employed in medicinal chemistry for the construction of cyclopropane-containing molecules, which are known for their unique biological activities and stability. Additionally, it serves as a protective group for amines during multi-step synthetic processes, enabling selective reactions in the presence of sensitive functional groups. Its application extends to the field of agrochemicals, where it contributes to the synthesis of novel pesticides and herbicides with enhanced efficacy.
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