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6-(N-benzyloxycarbonylamino)hexyl-O-(2,3,4-tri-O-benzyl-α-L-fucopyranosyl)-(1->3)-2-acetamido-4,6-O-benzylidene-2-deoxy-β-D-glucopyranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

171612-31-0

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  • 6-(N-benzyloxycarbonylamino)hexyl-O-(2,3,4-tri-O-benzyl-α-L-fucopyranosyl)-(1->3)-2-acetamido-4,6-O-benzylidene-2-deoxy-β-D-glucopyranoside

    Cas No: 171612-31-0

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  • 6-(N-benzyloxycarbonylamino)hexyl-O-(2,3,4-tri-O-benzyl-α-L-fucopyranosyl)-(1->3)-2-acetamido-4,6-O-benzylidene-2-deoxy-β-D-glucopyranoside

    Cas No: 171612-31-0

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171612-31-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 171612-31-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,1,6,1 and 2 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 171612-31:
(8*1)+(7*7)+(6*1)+(5*6)+(4*1)+(3*2)+(2*3)+(1*1)=110
110 % 10 = 0
So 171612-31-0 is a valid CAS Registry Number.

171612-31-0Relevant articles and documents

Synthesis of Sulfated Lex-Trisaccharides

Stahl, W.,Sprengard, U.,Kretzschmar, G.,Schmidt, D. W.,Kunz, H.

, p. 441 - 445 (1995)

The regioselective sulfation of a Lex-trisaccharide having free hydroxyl groups in 2-, 3- and 4- position of the galactose elucidated their different reactivities and gave mono- and disulfated Lex derivatives.

Large scale synthesis of linker-modified sialyl Lewis(X), Lewis(X) and N-acetyllactosamine

Kretzschmar, Gerhard,Stahl, Wilhelm

, p. 6341 - 6358 (2007/10/03)

The synthesis of sialyl-Lewis(X) (1b), Lewis(X) (2) and N- acetyllactosamine (3), each being attached to the 1β-O-(6-amino)hexyl handle, were scaled up to gram amounts to obtain sufficient material for thorough pharmaceutical evaluations and for derivatisations aiming at more potent selectin antagonists. The disaccharide 3 was synthesised from inexpensive lactose to provide a versatile building block, either to be used for alternative approaches to the Lewis type oligosaccharides, or to prepare polyvalent LacNAc templates to be further elaborated by glycosyltransferase reactions. All syntheses were directed to reasonable large scale procedures, especially by minimising the number of steps and the use of heavy metal salts in glycosylations.

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