92420-89-8 | 2,3,4-Tri-o-acetyl-alpha-d-glucuronic acid methyl ester, trichloroacetimidate

Packsize	Purity	Availability	Price	Discounted Price
1g	97%	in stock	$23.00	$17.00
5g	97%	in stock	$75.00	$53.00
10g	97%	in stock	$150.00	$105.00

Description

• Catalog Number: AB43555
• Chemical Name: 2,3,4-Tri-o-acetyl-alpha-d-glucuronic acid methyl ester, trichloroacetimidate
• CAS Number: 92420-89-8
• Molecular Formula: C15H18Cl3NO10
• Molecular Weight: 478.6631
• MDL Number: MFCD02094293
• SMILES: COC(=O)[C@H]1O[C@H](OC(=N)C(Cl)(Cl)Cl)[C@@H]([C@H]([C@@H]1OC(=O)C)OC(=O)C)OC(=O)C

Computed Properties

• Complexity: 680
• Covalently-Bonded Unit Count: 1
• Defined Atom Stereocenter Count: 5
• Heavy Atom Count: 29
• Hydrogen Bond Acceptor Count: 11
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 10
• XLogP3: 1.7

Upstream Synthesis Route

2,3,4-tri-O-acetyl-alpha-D-glucuronic acid methyl ester, trichloroacetimidate is a versatile compound widely used in chemical synthesis processes. Known for its ability to function as a powerful glycosyl donor, this compound plays a crucial role in the efficient and precise assembly of complex carbohydrate structures. Through its unique reactivity and selectivity, it facilitates the formation of glycosidic bonds with high efficiency, making it a valuable tool in synthesizing a wide range of bioactive compounds, natural products, and pharmaceutical intermediates. Its utility extends across various synthetic methodologies, including oligosaccharide synthesis, glycoconjugate synthesis, and carbohydrate-based drug development. By enabling the controlled and selective manipulation of carbohydrate molecules, this compound opens up new possibilities for the design and synthesis of novel molecules with diverse applications in the field of chemistry.

Literature

• Acetylated methyl glucopyranuronate trichloroacetimidate as a glycosyl donor for efficient synthesis of disaccharides.

  Carbohydrate research 20031031