Cas 334697-23-3,methyl 2-O-acetyl-3,4,6-tri-O-benzoyl-α-D-mannopyranosyl-(1->6)-2,4-di-O-benzoyl-3-O-tert-butyldimethylsilyl-α-D-mannopyranoside

334697-23-3

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Basic information

Product Name: methyl 2-O-acetyl-3,4,6-tri-O-benzoyl-α-D-mannopyranosyl-(1->6)-2,4-di-O-benzoyl-3-O-tert-butyldimethylsilyl-α-D-mannopyranoside
Synonyms: methyl 2-O-acetyl-3,4,6-tri-O-benzoyl-α-D-mannopyranosyl-(1->6)-2,4-di-O-benzoyl-3-O-tert-butyldimethylsilyl-α-D-mannopyranoside
CAS NO:334697-23-3
Molecular Formula:
Molecular Weight: 1033.17
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: methyl 2-O-acetyl-3,4,6-tri-O-benzoyl-α-D-mannopyranosyl-(1->6)-2,4-di-O-benzoyl-3-O-tert-butyldimethylsilyl-α-D-mannopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: methyl 2-O-acetyl-3,4,6-tri-O-benzoyl-α-D-mannopyranosyl-(1->6)-2,4-di-O-benzoyl-3-O-tert-butyldimethylsilyl-α-D-mannopyranoside(334697-23-3)
EPA Substance Registry System: methyl 2-O-acetyl-3,4,6-tri-O-benzoyl-α-D-mannopyranosyl-(1->6)-2,4-di-O-benzoyl-3-O-tert-butyldimethylsilyl-α-D-mannopyranoside(334697-23-3)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 334697-23-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 334697-23-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,4,6,9 and 7 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 334697-23:
(8*3)+(7*3)+(6*4)+(5*6)+(4*9)+(3*7)+(2*2)+(1*3)=163
163 % 10 = 3
So 334697-23-3 is a valid CAS Registry Number.

334697-23-3Upstream product

334697-23-3Downstream Products

334697-24-4 methyl 3,4,6-tri-O-benzoyl-α-D-mannopyranosyl-(1->6)-2,4-di-O-benzoyl-α-D-mannopyranoside

334697-23-3Relevant academic research and scientific papers

Efficient and practical syntheses of three pentasaccharides core structures corresponding to N-glycans

Du, Yuguo,Zhang, Meimei,Kong, Fanzuo

, p. 1757 - 1763 (2007/10/03)

Three branched pentasaccharide derivatives and one tetrasaccharide were synthesized efficiently. The advantages of this method include a one-pot facile synthesis of 3,6-differentially protected mannose building block and an efficient strategy for oligosac

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