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CAS

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6697-88-7

2,3,4,6-tetra-O-acetyl-1-n-butyl-β-D-glucopyranoside is a complex organic compound that belongs to the class of glycosides. It is a derivative of β-D-glucopyranoside, a monosaccharide, with four acetyl groups attached to the hydroxyl groups at the 2, 3, 4, and 6 positions, and a n-butyl group at the 1 position. 2,3,4,6-tetra-O-acetyl-1-n-butyl-β-D-glucopyranoside is characterized by its molecular formula C18H28O9 and a molecular weight of 388.41 g/mol. It is a white crystalline solid and is soluble in organic solvents such as chloroform and methanol. The compound is synthesized through a series of chemical reactions, including acetylation and alkylation, and is used in various applications, including as a protecting group in carbohydrate chemistry and as a potential intermediate in the synthesis of pharmaceuticals and other bioactive compounds. Its chemical structure and properties make it a valuable tool in the study and manipulation of complex carbohydrates.

6697-88-7

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6697-88-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6697-88-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,9 and 7 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6697-88:
(6*6)+(5*6)+(4*9)+(3*7)+(2*8)+(1*8)=147
147 % 10 = 7
So 6697-88-7 is a valid CAS Registry Number.

6697-88-7Relevant articles and documents

Synthesis of C7-C16-alkyl glycosides: Part I - Synthesis of alkyl D-glucopyranosides in the presence of tin (IV) chloride as a Lewis acid catalyst

Konstantinovic,Predojevic,Mojsilovic,Dimitrijevic,Milosevic

, p. 796 - 801 (2007/10/03)

The Lewis acid catalyzed glycosylation reaction of β-peracetylated sugar derivative (glucose) with fatty alkanols is used in a synthesis of C7-C16-alkyl glucopyranosides. The process occurs under the influence of tin (IV) chloride.

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