tert-Butyl (1-(hydroxymethyl)cyclopropyl)carbamate
97%
- Product Code: 104408
CAS:
107017-73-2
| Molecular Weight: | 187.24 g./mol | Molecular Formula: | C₉H₁₇NO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09749954 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, sealed, dry |
Product Description:
This chemical is primarily utilized in organic synthesis as a building block or intermediate for the preparation of more complex molecules. Its structure, featuring a cyclopropyl group and a carbamate moiety, makes it valuable in the development of pharmaceuticals, particularly in the synthesis of compounds with potential biological activity. The tert-butyl group provides steric protection, allowing selective reactions at other functional groups. It is often employed in peptide chemistry and drug discovery, where it can serve as a protecting group for amines, ensuring controlled reactivity during multi-step synthesis. Additionally, its cyclopropyl ring is of interest in medicinal chemistry due to its ability to influence the conformational and pharmacological properties of target molecules.
Product Specification:
| Test | Specification |
|---|---|
| Purity (%) | 96.5-100 |
| Melting Point (Degree Celsius) | 81-85 |
| Appearance | Very Pale Yellow - Pale Yellow Crystal - Powder |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $69.98 |
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| 5.000 | 10-20 days | $309.02 |
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| 25.000 | 10-20 days | $1,286.81 |
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tert-Butyl (1-(hydroxymethyl)cyclopropyl)carbamate
This chemical is primarily utilized in organic synthesis as a building block or intermediate for the preparation of more complex molecules. Its structure, featuring a cyclopropyl group and a carbamate moiety, makes it valuable in the development of pharmaceuticals, particularly in the synthesis of compounds with potential biological activity. The tert-butyl group provides steric protection, allowing selective reactions at other functional groups. It is often employed in peptide chemistry and drug discovery, where it can serve as a protecting group for amines, ensuring controlled reactivity during multi-step synthesis. Additionally, its cyclopropyl ring is of interest in medicinal chemistry due to its ability to influence the conformational and pharmacological properties of target molecules.
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