(S)-(-)-Glycidyl trityl ether
97%
- Product Code: 234260
Alias:
(S)-tritylglycidyl ether; triphenyl-(S)-glycidyl ether
CAS:
129940-50-7
Molecular Weight: | 316.39 g./mol | Molecular Formula: | C₂₂H₂₀O₂ |
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EC Number: | MDL Number: | MFCD00273373 | |
Melting Point: | 99-102 °C(lit.) | Boiling Point: | |
Density: | Storage Condition: | Room temperature, dry, sealed |
Product Description:
Used as a chiral building block in organic synthesis, particularly in the preparation of enantiomerically pure compounds. It serves as a protective group for alcohols in nucleoside and carbohydrate chemistry due to the stability of the trityl group under various reaction conditions. The epoxide ring allows for regioselective and stereoselective ring-opening reactions, enabling the introduction of functionalized side chains in pharmaceutical intermediates. Commonly employed in the synthesis of beta-blockers and other bioactive molecules where stereochemistry is critical. Its trityl moiety provides lipophilicity, aiding in purification and separation processes such as chromatography.
Sizes / Availability / Pricing:
Size | Availability | Price | Quantity |
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1g | 10-20 days | ฿150.00 |
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5g | 10-20 days | ฿350.00 |
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25g | 10-20 days | ฿990.00 |
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(S)-(-)-Glycidyl trityl ether
Used as a chiral building block in organic synthesis, particularly in the preparation of enantiomerically pure compounds. It serves as a protective group for alcohols in nucleoside and carbohydrate chemistry due to the stability of the trityl group under various reaction conditions. The epoxide ring allows for regioselective and stereoselective ring-opening reactions, enabling the introduction of functionalized side chains in pharmaceutical intermediates. Commonly employed in the synthesis of beta-blockers and other bioactive molecules where stereochemistry is critical. Its trityl moiety provides lipophilicity, aiding in purification and separation processes such as chromatography.
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