4-(1-((tert-Butoxycarbonyl)amino)ethyl)benzoic acid
≥95%
- Product Code: 118480
CAS:
895577-21-6
| Molecular Weight: | 265.31 g./mol | Molecular Formula: | C₁₄H₁₉NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD11505982 | |
| Melting Point: | Boiling Point: | 359.9°C at 760 mmHg | |
| Density: | Storage Condition: | room temperature, stored under inert gas |
Product Description:
This chemical is primarily used in the field of organic synthesis, particularly in the development of pharmaceuticals. It serves as a key intermediate in the production of various active pharmaceutical ingredients (APIs). Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group, makes it valuable in peptide synthesis, where the Boc group is used to protect amines during the construction of complex peptide chains. Additionally, it is employed in the preparation of small molecule drugs, where its benzoic acid moiety can be further modified to create biologically active compounds. Its role in medicinal chemistry is significant, as it aids in the efficient and selective synthesis of target molecules with potential therapeutic applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿2,700.00 |
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| 0.250 | 10-20 days | ฿5,391.00 |
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4-(1-((tert-Butoxycarbonyl)amino)ethyl)benzoic acid
This chemical is primarily used in the field of organic synthesis, particularly in the development of pharmaceuticals. It serves as a key intermediate in the production of various active pharmaceutical ingredients (APIs). Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group, makes it valuable in peptide synthesis, where the Boc group is used to protect amines during the construction of complex peptide chains. Additionally, it is employed in the preparation of small molecule drugs, where its benzoic acid moiety can be further modified to create biologically active compounds. Its role in medicinal chemistry is significant, as it aids in the efficient and selective synthesis of target molecules with potential therapeutic applications.
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