(S)-1-((Benzyloxy)carbonyl)pyrrolidine-3-carboxylic acid
97%
- Product Code: 37955
CAS:
192214-00-9
Molecular Weight: | 249.26 g./mol | Molecular Formula: | C₁₃H₁₅NO₄ |
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EC Number: | MDL Number: | MFCD09608053 | |
Melting Point: | Boiling Point: | 432.3°C at 760 mmHg | |
Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This compound is primarily used in the synthesis of peptides and pharmaceutical intermediates. It serves as a chiral building block in organic chemistry, enabling the creation of complex molecules with specific stereochemistry. Its structure is particularly valuable in the development of drugs targeting neurological disorders, as it can be incorporated into active pharmaceutical ingredients (APIs) that interact with receptors in the brain. Additionally, it is employed in the preparation of proline derivatives, which are essential in the production of protease inhibitors and other therapeutic agents. Its benzyloxycarbonyl (Cbz) protecting group is useful in peptide synthesis, as it can be easily removed under mild conditions, making it a versatile tool in medicinal chemistry and drug discovery.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.250 | 10-20 days | $103.16 |
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1.000 | 10-20 days | $246.68 |
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5.000 | 10-20 days | $741.92 |
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10.000 | 10-20 days | $1,196.04 |
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(S)-1-((Benzyloxy)carbonyl)pyrrolidine-3-carboxylic acid
This compound is primarily used in the synthesis of peptides and pharmaceutical intermediates. It serves as a chiral building block in organic chemistry, enabling the creation of complex molecules with specific stereochemistry. Its structure is particularly valuable in the development of drugs targeting neurological disorders, as it can be incorporated into active pharmaceutical ingredients (APIs) that interact with receptors in the brain. Additionally, it is employed in the preparation of proline derivatives, which are essential in the production of protease inhibitors and other therapeutic agents. Its benzyloxycarbonyl (Cbz) protecting group is useful in peptide synthesis, as it can be easily removed under mild conditions, making it a versatile tool in medicinal chemistry and drug discovery.
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