3-((tert-Butoxycarbonyl)amino)-3-(3,4-dimethoxyphenyl)propanoic acid
95%
- Product Code: 104532
CAS:
284492-37-1
Molecular Weight: | 325.36 g./mol | Molecular Formula: | C₁₆H₂₃NO₆ |
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EC Number: | MDL Number: | MFCD01931739 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | Room temperature, sealed, dry |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in the preparation of peptide derivatives and other bioactive molecules. Its tert-butoxycarbonyl (Boc) protecting group is commonly employed to safeguard the amino functionality during complex chemical reactions, ensuring selective transformations. The presence of the 3,4-dimethoxyphenyl moiety makes it a valuable intermediate in the synthesis of compounds with potential pharmacological activity, such as those targeting neurological or cardiovascular disorders. Additionally, it serves as a building block in the development of chiral molecules, enabling the creation of enantiomerically pure substances for use in drug discovery and development.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿6,480.00 |
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0.250 | 10-20 days | ฿12,870.00 |
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1.000 | 10-20 days | ฿25,740.00 |
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3-((tert-Butoxycarbonyl)amino)-3-(3,4-dimethoxyphenyl)propanoic acid
This compound is primarily utilized in organic synthesis, particularly in the preparation of peptide derivatives and other bioactive molecules. Its tert-butoxycarbonyl (Boc) protecting group is commonly employed to safeguard the amino functionality during complex chemical reactions, ensuring selective transformations. The presence of the 3,4-dimethoxyphenyl moiety makes it a valuable intermediate in the synthesis of compounds with potential pharmacological activity, such as those targeting neurological or cardiovascular disorders. Additionally, it serves as a building block in the development of chiral molecules, enabling the creation of enantiomerically pure substances for use in drug discovery and development.
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