(R)-1,2,3,4-TETRAHYDRO-QUINOLINE-2-CARBOXYLIC ACID
≥95%
- Product Code: 37300
CAS:
92977-00-9
| Molecular Weight: | 177.2 g./mol | Molecular Formula: | C₁₀H₁₁NO₂ |
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| Density: | Storage Condition: | 2-8℃ |
Product Description:
(R)-1,2,3,4-Tetrahydro-quinoline-2-carboxylic acid is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmaceutical compounds. Its chiral structure makes it valuable for the development of enantiomerically pure drugs, particularly those targeting neurological and cardiovascular disorders. The compound is often employed in the preparation of inhibitors for enzymes like ACE (angiotensin-converting enzyme) and other biologically relevant targets. Additionally, it serves as a building block in the creation of peptidomimetics, which are used to mimic the structure and function of peptides for therapeutic applications. Its role in organic synthesis also extends to the production of ligands for asymmetric catalysis, aiding in the creation of complex molecules with high stereochemical control.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿12,789.00 |
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| 0.250 | 10-20 days | ฿19,179.00 |
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(R)-1,2,3,4-TETRAHYDRO-QUINOLINE-2-CARBOXYLIC ACID
(R)-1,2,3,4-Tetrahydro-quinoline-2-carboxylic acid is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmaceutical compounds. Its chiral structure makes it valuable for the development of enantiomerically pure drugs, particularly those targeting neurological and cardiovascular disorders. The compound is often employed in the preparation of inhibitors for enzymes like ACE (angiotensin-converting enzyme) and other biologically relevant targets. Additionally, it serves as a building block in the creation of peptidomimetics, which are used to mimic the structure and function of peptides for therapeutic applications. Its role in organic synthesis also extends to the production of ligands for asymmetric catalysis, aiding in the creation of complex molecules with high stereochemical control.
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