(E)-4-(Benzylamino)-4-oxobut-2-enoic acid
95%
- Product Code: 87136
CAS:
685543-77-5
| Molecular Weight: | 205.21 g./mol | Molecular Formula: | C₁₁H₁₁NO₃ |
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| EC Number: | MDL Number: | MFCD00185898 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry, airtight |
Product Description:
This chemical is primarily utilized in the field of organic synthesis, where it serves as a valuable intermediate for the preparation of more complex molecules. Its structure, featuring both an amide and a carboxylic acid functional group, makes it suitable for coupling reactions, enabling the formation of peptide bonds or other amide linkages. This property is particularly useful in the development of pharmaceuticals, where it can be employed to create bioactive compounds or drug candidates. Additionally, its conjugated double bond allows it to participate in cyclization reactions, contributing to the synthesis of heterocyclic compounds, which are often found in medicinal chemistry. In research, it may also be used to study reaction mechanisms or to develop new synthetic methodologies.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿1,728.00 |
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(E)-4-(Benzylamino)-4-oxobut-2-enoic acid
This chemical is primarily utilized in the field of organic synthesis, where it serves as a valuable intermediate for the preparation of more complex molecules. Its structure, featuring both an amide and a carboxylic acid functional group, makes it suitable for coupling reactions, enabling the formation of peptide bonds or other amide linkages. This property is particularly useful in the development of pharmaceuticals, where it can be employed to create bioactive compounds or drug candidates. Additionally, its conjugated double bond allows it to participate in cyclization reactions, contributing to the synthesis of heterocyclic compounds, which are often found in medicinal chemistry. In research, it may also be used to study reaction mechanisms or to develop new synthetic methodologies.
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