(S)-Tetrahydropyridazine-1,2,3-tricarboxylic acid 1,2-di-tert-butyl ester
98%
- Product Code: 86449
CAS:
156699-39-7
| Molecular Weight: | 330.38 g./mol | Molecular Formula: | C₁₅H₂₆N₂O₆ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD23099733 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry, sealed |
Product Description:
This compound is primarily utilized in the field of organic synthesis, particularly as a chiral building block for the development of complex molecules. Its structure, featuring a tetrahydropyridazine core and tert-butyl ester groups, makes it valuable for creating enantiomerically pure compounds, which are essential in pharmaceutical research. The compound is often employed in asymmetric synthesis to introduce chirality into target molecules, aiding in the production of drugs with specific stereochemical requirements. Additionally, it serves as an intermediate in the synthesis of bioactive compounds, including potential therapeutic agents for neurological and cardiovascular diseases. Its stability and reactivity under various conditions make it a versatile tool in medicinal chemistry.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to off-white Solid |
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | $32.14 |
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| 1.000 | 10-20 days | $95.43 |
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| 5.000 | 10-20 days | $445.00 |
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(S)-Tetrahydropyridazine-1,2,3-tricarboxylic acid 1,2-di-tert-butyl ester
This compound is primarily utilized in the field of organic synthesis, particularly as a chiral building block for the development of complex molecules. Its structure, featuring a tetrahydropyridazine core and tert-butyl ester groups, makes it valuable for creating enantiomerically pure compounds, which are essential in pharmaceutical research. The compound is often employed in asymmetric synthesis to introduce chirality into target molecules, aiding in the production of drugs with specific stereochemical requirements. Additionally, it serves as an intermediate in the synthesis of bioactive compounds, including potential therapeutic agents for neurological and cardiovascular diseases. Its stability and reactivity under various conditions make it a versatile tool in medicinal chemistry.
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