AD-mix-α
98%
- Product Code: 53591
CAS:
153130-59-7
Molecular Weight: | 778.42 g./mol | Molecular Formula: | C₄₈H₅₄N₆O₄ |
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EC Number: | MDL Number: | MFCD00197840 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | room temperature |
Product Description:
AD-mix-α is widely used in organic synthesis for the enantioselective dihydroxylation of alkenes. This reaction is crucial for producing chiral diols, which are valuable intermediates in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. The mix facilitates the introduction of two hydroxyl groups across a double bond in a highly stereoselective manner, often leading to high enantiomeric excesses. It is particularly favored in the preparation of complex molecules where precise stereochemistry is essential. Additionally, AD-mix-α is employed in academic research to explore new synthetic pathways and develop novel catalytic processes. Its ease of use and consistent performance make it a reliable tool for chemists aiming to achieve high selectivity in their synthetic endeavors.
Product Specification:
Test | Specification |
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APPEARANCE | Yellow solid |
PURITY | 97.5-100 |
Infrared spectrum | Conforms to Structure |
K2CO3 | 29.4 |
K3FeCN6 | 70 |
K2OsO2OH4 | 0.052 |
DHQD2PHAL | 0.552 |
WATER | 0 1% |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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1.000 | 10-20 days | $17.70 |
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5.000 | 10-20 days | $58.99 |
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25.000 | 10-20 days | $248.15 |
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AD-mix-α
AD-mix-α is widely used in organic synthesis for the enantioselective dihydroxylation of alkenes. This reaction is crucial for producing chiral diols, which are valuable intermediates in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. The mix facilitates the introduction of two hydroxyl groups across a double bond in a highly stereoselective manner, often leading to high enantiomeric excesses. It is particularly favored in the preparation of complex molecules where precise stereochemistry is essential. Additionally, AD-mix-α is employed in academic research to explore new synthetic pathways and develop novel catalytic processes. Its ease of use and consistent performance make it a reliable tool for chemists aiming to achieve high selectivity in their synthetic endeavors.
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