CAS 849420-02-6
:a-D-Mannopyranoside,2-chloroethyl, tetraacetate (9CI)
Description:
α-D-Mannopyranoside, 2-chloroethyl, tetraacetate (9CI) is a synthetic carbohydrate derivative characterized by its structure, which includes a mannopyranoside backbone modified with a 2-chloroethyl group and four acetyl groups. This compound is typically used in organic synthesis and carbohydrate chemistry due to its reactivity and ability to participate in glycosylation reactions. The presence of the tetraacetate moiety enhances its stability and solubility in organic solvents, making it suitable for various chemical applications. The 2-chloroethyl group can serve as a leaving group in nucleophilic substitution reactions, facilitating further modifications. Additionally, this compound may exhibit specific biological activities, although detailed biological data may vary. Its CAS number, 849420-02-6, allows for precise identification in chemical databases. Overall, α-D-Mannopyranoside, 2-chloroethyl, tetraacetate is a valuable compound in the field of synthetic organic chemistry, particularly in the development of glycosylated compounds and other derivatives.
Formula:C16H23ClO10
Synonyms:- 2-Chloroethyl-2,3,4,6-tetra-O-acetyl-a-D-mannopyranoside
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Found 3 products.
2-Chloroethyl 2,3,4,6-tetra-O-acetyl-α-D-mannopyranoside
CAS:<p>2-Chloroethyl 2,3,4,6-tetra-O-acetyl-α-D-mannopyranoside</p>Molecular weight:410.80g/mol2-Chloroethyl-2,3,4,6-tetra-O-acetyl-a-D-mannopyranoside
CAS:<p>2-Chloroethyl-2,3,4,6-tetra-O-acetyl-a-D-mannopyranoside is a glycosylation agent. It can be used to modify glycoproteins and glycolipids by reacting with the hydroxyl groups of saccharides. 2-Chloroethyl-2,3,4,6-tetra-O-acetyl-a-D-mannopyranoside is also used for the synthesis of oligosaccharides and monosaccharides. This product has been shown to react with proteins at a rate of around 1% per hour in aqueous media at pH 7.5 at room temperature.</p>Formula:C16H23ClO10Purity:Min. 95%Molecular weight:410.8 g/mol
