2-((tert-Butoxycarbonyl)amino)-2-(p-tolyl)acetic acid
95%
- Product Code: 41184
CAS:
28044-77-1
| Molecular Weight: | 265.3050 g./mol | Molecular Formula: | C₁₄H₁₉NO₄ |
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| EC Number: | MDL Number: | MFCD03789598 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily used in organic synthesis as a building block for the preparation of more complex molecules, particularly in pharmaceutical research. It serves as an intermediate in the synthesis of peptides and other biologically active compounds, where the tert-butoxycarbonyl (Boc) group acts as a protecting group for amines during multi-step reactions. Its structure, featuring a p-tolyl group, makes it valuable in the development of compounds with specific aromatic interactions, which can be crucial in drug design. Additionally, it is utilized in the study of enzyme inhibitors and receptor ligands, contributing to the exploration of therapeutic agents for various diseases. Its stability and reactivity under controlled conditions make it a preferred choice in medicinal chemistry workflows.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿2,673.00 |
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2-((tert-Butoxycarbonyl)amino)-2-(p-tolyl)acetic acid
This chemical is primarily used in organic synthesis as a building block for the preparation of more complex molecules, particularly in pharmaceutical research. It serves as an intermediate in the synthesis of peptides and other biologically active compounds, where the tert-butoxycarbonyl (Boc) group acts as a protecting group for amines during multi-step reactions. Its structure, featuring a p-tolyl group, makes it valuable in the development of compounds with specific aromatic interactions, which can be crucial in drug design. Additionally, it is utilized in the study of enzyme inhibitors and receptor ligands, contributing to the exploration of therapeutic agents for various diseases. Its stability and reactivity under controlled conditions make it a preferred choice in medicinal chemistry workflows.
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