65291-30-7 | (R)-(+)-Trityl glycidyl ether

Packsize	Purity	Availability	Price	Discounted Price
1g	97%	in stock	$18.00	$13.00
5g	97%	in stock	$22.00	$15.00
25g	97%	in stock	$63.00	$44.00
100g	97%	in stock	$209.00	$146.00

Description

• Catalog Number: AB42874
• Chemical Name: (R)-(+)-Trityl glycidyl ether
• CAS Number: 65291-30-7
• Molecular Formula: C22H20O2
• Molecular Weight: 316.393
• MDL Number: MFCD00273368
• SMILES: O1C[C@@H]1COC(c1ccccc1)(c1ccccc1)c1ccccc1

Upstream Synthesis Route

(R)-(+)-Trityl glycidyl ether is a versatile and valuable compound in chemical synthesis due to its unique properties and reactivity. This chiral epoxide derivative is widely used as a protecting group for alcohols in organic synthesis. In particular, it is commonly employed in the protection of hydroxyl groups in complex molecules to control the regioselectivity and stereochemistry of subsequent chemical reactions.One of the key applications of (R)-(+)-Trityl glycidyl ether is in the selective protection of the primary hydroxyl group in polyols and carbohydrates. By using this compound as a protecting group, chemists can mask the reactive hydroxyl functionality while allowing other functional groups to participate in desired reactions. This strategy is crucial in the synthesis of natural products, pharmaceuticals, and advanced materials where precise control over functional group transformations is essential.Furthermore, (R)-(+)-Trityl glycidyl ether exhibits excellent stability under a wide range of reaction conditions, making it compatible with various synthetic methods and reagents. Its ease of installation and removal, along with its compatibility with common chemical reactions, make it a valuable tool for chemists in the development of complex molecular architectures.In summary, the application of (R)-(+)-Trityl glycidyl ether in chemical synthesis offers chemists a reliable and efficient method for protecting hydroxyl groups and controlling the reactivity of complex molecules. This versatile compound plays a crucial role in enabling the synthesis of intricate organic compounds with high precision and selectivity.