(S)-tert-Butyl 2-(hydroxymethyl)-2,5-dihydro-1H-pyrrole-1-carboxylate
97%
- Product Code: 38183
CAS:
205444-34-4
| Molecular Weight: | 199.2469 g./mol | Molecular Formula: | C₁₀H₁₇NO₃ |
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| EC Number: | MDL Number: | MFCD18074315 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in organic synthesis as a chiral building block for the preparation of more complex molecules. Its structure, featuring a protected hydroxymethyl group and a pyrrole ring, makes it valuable in the development of pharmaceuticals, particularly in the synthesis of biologically active compounds. The tert-butyloxycarbonyl (Boc) protecting group ensures stability during reactions, allowing selective transformations. It is often employed in the synthesis of pyrrole-containing drugs, peptidomimetics, and other heterocyclic compounds with potential therapeutic applications. Additionally, its chiral nature enables the creation of enantiomerically pure products, which is crucial in drug development to ensure efficacy and reduce side effects.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿3,474.00 |
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(S)-tert-Butyl 2-(hydroxymethyl)-2,5-dihydro-1H-pyrrole-1-carboxylate
This compound is primarily utilized in organic synthesis as a chiral building block for the preparation of more complex molecules. Its structure, featuring a protected hydroxymethyl group and a pyrrole ring, makes it valuable in the development of pharmaceuticals, particularly in the synthesis of biologically active compounds. The tert-butyloxycarbonyl (Boc) protecting group ensures stability during reactions, allowing selective transformations. It is often employed in the synthesis of pyrrole-containing drugs, peptidomimetics, and other heterocyclic compounds with potential therapeutic applications. Additionally, its chiral nature enables the creation of enantiomerically pure products, which is crucial in drug development to ensure efficacy and reduce side effects.
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