(S)-4-(tert-Butoxy)-2-methyl-4-oxobutanoic acid
98%
- Product Code: 38502
CAS:
182007-75-6
| Molecular Weight: | 188.22 g./mol | Molecular Formula: | C₉H₁₆O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD19382513 | |
| Melting Point: | Boiling Point: | 281.9±23.0 °C(Predicted) | |
| Density: | 1.071±0.06 g/cm3(Predicted) | Storage Condition: | Room temperature, sealed, dry |
Product Description:
This chemical is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of chiral compounds. Its structure, featuring a tert-butoxy group and a methyl substituent, makes it a valuable building block for creating complex molecules with specific stereochemistry. It is often employed in the production of active pharmaceutical ingredients (APIs) where precise chiral control is essential. Additionally, it finds application in organic synthesis for constructing ester and carboxylic acid derivatives, which are key components in various drug discovery and development processes. Its stability and reactivity under controlled conditions make it a reliable reagent in medicinal chemistry and fine chemical manufacturing.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿2,061.00 |
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| 1.000 | 10-20 days | ฿5,562.00 |
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| 5.000 | 10-20 days | ฿19,449.00 |
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(S)-4-(tert-Butoxy)-2-methyl-4-oxobutanoic acid
This chemical is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of chiral compounds. Its structure, featuring a tert-butoxy group and a methyl substituent, makes it a valuable building block for creating complex molecules with specific stereochemistry. It is often employed in the production of active pharmaceutical ingredients (APIs) where precise chiral control is essential. Additionally, it finds application in organic synthesis for constructing ester and carboxylic acid derivatives, which are key components in various drug discovery and development processes. Its stability and reactivity under controlled conditions make it a reliable reagent in medicinal chemistry and fine chemical manufacturing.
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