(R)-3-Methyl-pyrrolidine-1,3-dicarboxylic acid 1-benzyl ester
95%
- Product Code: 123679
CAS:
1412254-17-1
| Molecular Weight: | 263.29 g./mol | Molecular Formula: | C₁₄H₁₇NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28098161 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, sealed, dry |
Product Description:
This compound is primarily utilized in the field of organic synthesis, particularly as a chiral building block for the preparation of more complex molecules. Its structure, featuring a pyrrolidine ring and a benzyl ester group, makes it valuable in the development of pharmaceuticals and biologically active compounds. It is often employed in asymmetric synthesis to introduce chirality into target molecules, which is crucial for the production of enantiomerically pure drugs. Additionally, it serves as an intermediate in the synthesis of various alkaloids and other nitrogen-containing heterocycles, which are important in medicinal chemistry and drug discovery. Its ester group can also be selectively modified or removed, allowing for further functionalization in multi-step synthetic routes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿8,100.00 |
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(R)-3-Methyl-pyrrolidine-1,3-dicarboxylic acid 1-benzyl ester
This compound is primarily utilized in the field of organic synthesis, particularly as a chiral building block for the preparation of more complex molecules. Its structure, featuring a pyrrolidine ring and a benzyl ester group, makes it valuable in the development of pharmaceuticals and biologically active compounds. It is often employed in asymmetric synthesis to introduce chirality into target molecules, which is crucial for the production of enantiomerically pure drugs. Additionally, it serves as an intermediate in the synthesis of various alkaloids and other nitrogen-containing heterocycles, which are important in medicinal chemistry and drug discovery. Its ester group can also be selectively modified or removed, allowing for further functionalization in multi-step synthetic routes.
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