(R)-()-Glycidyl trityl ether

98%

Reagent Code: #229858
label
Alias (R)-Glycidyl Trianthyl Ether
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CAS Number 65291-30-7

science Other reagents with same CAS 65291-30-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 316.39 g/mol
Formula C₂₂H₂₀O₂
badge Registry Numbers
MDL Number MFCD00273368
thermostat Physical Properties
Melting Point 99-102 °C(lit.)
inventory_2 Storage & Handling
Storage Room temperature, dry, sealed

description Product Description

Used as a chiral protecting group in organic synthesis, particularly for the protection of alcohols during multi-step reactions. Its trityl group provides steric bulk, enhancing selectivity in asymmetric synthesis. Commonly applied in the preparation of enantiomerically pure pharmaceuticals and fine chemicals. Stable under basic conditions and removable under mild acidic conditions, making it suitable for peptide and nucleoside chemistry. Also employed in the synthesis of chiral polymers and functionalized resins for chromatography.

Available Sizes & Pricing

Size Availability Unit Price Quantity
5g
10-20 days ฿1,240.00
25g
10-20 days ฿4,770.00
100g
10-20 days ฿15,730.00
(R)-()-Glycidyl trityl ether
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Used as a chiral protecting group in organic synthesis, particularly for the protection of alcohols during multi-step reactions. Its trityl group provides steric bulk, enhancing selectivity in asymmetric synthesis. Commonly applied in the preparation of enantiomerically pure pharmaceuticals and fine chemicals. Stable under basic conditions and removable under mild acidic conditions, making it suitable for peptide and nucleoside chemistry. Also employed in the synthesis of chiral polymers and functionaliz

Used as a chiral protecting group in organic synthesis, particularly for the protection of alcohols during multi-step reactions. Its trityl group provides steric bulk, enhancing selectivity in asymmetric synthesis. Commonly applied in the preparation of enantiomerically pure pharmaceuticals and fine chemicals. Stable under basic conditions and removable under mild acidic conditions, making it suitable for peptide and nucleoside chemistry. Also employed in the synthesis of chiral polymers and functionalized resins for chromatography.

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