(S)-3-hydroxy-2-(2,4,6-triisopropylphenylsulfonamido)propanoic acid
95%
- Product Code: 60725
CAS:
159155-05-2
| Molecular Weight: | 371.49 g./mol | Molecular Formula: | C₁₈H₂₉NO₅S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD31652397 | |
| Melting Point: | Boiling Point: | 512.9±60.0 °C(Predicted) | |
| Density: | 1.176±0.06 g/cm3(Predicted) | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the field of organic synthesis as a chiral building block or intermediate. Its structure, featuring a sulfonamido group and a hydroxy acid moiety, makes it valuable for constructing complex molecules with high stereochemical control. It is often employed in the synthesis of pharmaceuticals, particularly in the development of enantiomerically pure drugs, where its chiral center plays a critical role in ensuring the desired biological activity. Additionally, it can be used in peptide chemistry to introduce specific functional groups or stereochemistry into peptide chains. Its sulfonamide group also contributes to its potential use in designing enzyme inhibitors or receptor-targeted compounds.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | Ft151,268.48 |
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| 0.250 | 10-20 days | Ft264,719.83 |
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| 1.000 | 10-20 days | Ft529,439.67 |
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(S)-3-hydroxy-2-(2,4,6-triisopropylphenylsulfonamido)propanoic acid
This compound is primarily utilized in the field of organic synthesis as a chiral building block or intermediate. Its structure, featuring a sulfonamido group and a hydroxy acid moiety, makes it valuable for constructing complex molecules with high stereochemical control. It is often employed in the synthesis of pharmaceuticals, particularly in the development of enantiomerically pure drugs, where its chiral center plays a critical role in ensuring the desired biological activity. Additionally, it can be used in peptide chemistry to introduce specific functional groups or stereochemistry into peptide chains. Its sulfonamide group also contributes to its potential use in designing enzyme inhibitors or receptor-targeted compounds.
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