Cas 1240293-92-8,N4-{O-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-(1->2)-O-α-D-mannopyranosyl-(1->3)-[O-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-(1->2)-O-α-D-mannopyranosyl-(1->6)]-O-β-D-mannopyranosyl-(1->4)-O-(2-acetamido-3,6-di-O-benzyl-2-deoxy-β-D-glucopyranosyl)-(1->4)-(2-acetamido-3,6-di-O-benzyl-2-deoxy-β-D-glucopyranosyl)}-N2-benzyloxycarbonyl-L-asparagine tert-butyl ester

1240293-92-8

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Basic information

Product Name: N4-{O-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-(1->2)-O-α-D-mannopyranosyl-(1->3)-[O-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-(1->2)-O-α-D-mannopyranosyl-(1->6)]-O-β-D-mannopyranosyl-(1->4)-O-(2-acetamido-3,6-di-O-benzyl-2-deoxy-β-D-glucopyranosyl)-(1->4)-(2-acetamido-3,6-di-O-benzyl-2-deoxy-β-D-glucopyranosyl)}-N2-benzyloxycarbonyl-L-asparagine tert-butyl ester
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CAS NO:1240293-92-8
Molecular Formula:
Molecular Weight: 1982.07
EINECS: N/A
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Mol File: 1240293-92-8.mol

Chemical Properties

Melting Point: N/A
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Refractive Index: N/A
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Solubility: N/A
CAS DataBase Reference: N4-{O-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-(1->2)-O-α-D-mannopyranosyl-(1->3)-[O-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-(1->2)-O-α-D-mannopyranosyl-(1->6)]-O-β-D-mannopyranosyl-(1->4)-O-(2-acetamido-3,6-di-O-benzyl-2-deoxy-β-D-glucopyranosyl)-(1->4)-(2-acetamido-3,6-di-O-benzyl-2-deoxy-β-D-glucopyranosyl)}-N2-benzyloxycarbonyl-L-asparagine tert-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: N4-{O-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-(1->2)-O-α-D-mannopyranosyl-(1->3)-[O-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-(1->2)-O-α-D-mannopyranosyl-(1->6)]-O-β-D-mannopyranosyl-(1->4)-O-(2-acetamido-3,6-di-O-benzyl-2-deoxy-β-D-glucopyranosyl)-(1->4)-(2-acetamido-3,6-di-O-benzyl-2-deoxy-β-D-glucopyranosyl)}-N2-benzyloxycarbonyl-L-asparagine tert-butyl ester(1240293-92-8)
EPA Substance Registry System: N4-{O-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-(1->2)-O-α-D-mannopyranosyl-(1->3)-[O-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-(1->2)-O-α-D-mannopyranosyl-(1->6)]-O-β-D-mannopyranosyl-(1->4)-O-(2-acetamido-3,6-di-O-benzyl-2-deoxy-β-D-glucopyranosyl)-(1->4)-(2-acetamido-3,6-di-O-benzyl-2-deoxy-β-D-glucopyranosyl)}-N2-benzyloxycarbonyl-L-asparagine tert-butyl ester(1240293-92-8)

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Hazardous Substances Data: 1240293-92-8(Hazardous Substances Data)

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N4-{O-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-(1->2)-O-α-D-mannopyranosyl-(1->3)-[O-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-(1->2)-O-α-D-mannopyranosyl-(1->6)]-O-β-D-mannopyranosyl-(1->4)-O-(2-acetamido-3,6-di-O-benzyl-2-deoxy-β-D-glucopyranosyl)-(1->4)-(2-acetamido-3,6-di-O-benzyl-2-deoxy-β-D-glucopyranosyl)}-N2-benzyloxycarbonyl-L-asparagine tert-butyl ester
Cas No: 1240293-92-8
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N4-{O-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-(1->2)-O-α-D-mannopyranosyl-(1->3)-[O-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-(1->2)-O-α-D-mannopyranosyl-(1->6)]-O-β-D-mannopyranosyl-(1->4)-O-(2-acetamido-3,6-di-O-benzyl-2-deoxy-β-D-glucopyranosyl)-(1->4)-(2-acetamido-3,6-di-O-benzyl-2-deoxy-β-D-glucopyranosyl)}-N2-benzyloxycarbonyl-L-asparagine tert-butyl ester
Cas No: 1240293-92-8
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1240293-92-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1240293-92-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,0,2,9 and 3 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1240293-92:
(9*1)+(8*2)+(7*4)+(6*0)+(5*2)+(4*9)+(3*3)+(2*9)+(1*2)=128
128 % 10 = 8
So 1240293-92-8 is a valid CAS Registry Number.

1240293-92-8Upstream product

47307-26-6 (S)-2-benzyloxycarbonylamino-succinic acid 1-tert-butyl ester

1240293-92-8Downstream Products

1240293-92-8Relevant articles and documents

Synthesis of an Fmoc-Asn-heptasaccharide building block and its application to chemoenzymatic glycopeptide synthesis

Mezzato, Stefano,Unverzagt, Carlo

, p. 1306 - 1315 (2010)

The Fmoc-protected heptasaccharide asparagine building block β-GlcNAc-(1→2)-α-Man-(1→3)-[β-GlcNAc-(1→2) -α-Man-(1→6)]β-Man-(1→4)-β-GlcNAc-(1→4) -β-GlcNAc-(Fmoc)Asn was obtained by chemical synthesis. Two flexible strategies were developed with optimized c

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