Cas 1365547-48-3,ethyl-(3,6-di-O-allyl-4-O-benzyl-β-D-glucopyranosyl)-(1->4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside

1365547-48-3

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Basic information

Product Name: ethyl-(3,6-di-O-allyl-4-O-benzyl-β-D-glucopyranosyl)-(1->4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside
Synonyms:
CAS NO:1365547-48-3
Molecular Formula:
Molecular Weight: 866.042
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: ethyl-(3,6-di-O-allyl-4-O-benzyl-β-D-glucopyranosyl)-(1->4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: ethyl-(3,6-di-O-allyl-4-O-benzyl-β-D-glucopyranosyl)-(1->4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside(1365547-48-3)
EPA Substance Registry System: ethyl-(3,6-di-O-allyl-4-O-benzyl-β-D-glucopyranosyl)-(1->4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside(1365547-48-3)

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: 1365547-48-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1365547-48-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,5,5,4 and 7 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1365547-48:
(9*1)+(8*3)+(7*6)+(6*5)+(5*5)+(4*4)+(3*7)+(2*4)+(1*8)=183
183 % 10 = 3
So 1365547-48-3 is a valid CAS Registry Number.

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1365547-48-3Relevant academic research and scientific papers

Synthesis of fully O-benzylated N-linked core pentasaccharide glycosyl azide

Kalmar, Laszlo,Agoston, Karoly,Szurmai, Zoltan,Doencz, Boglarka,Kerekgyarto, Janos

, p. 203 - 219 (2012/07/03)

The fully O-benzylated pentasaccharide glycosyl azide representing the common core structure of N-glycans was synthesized. The β-mannosidic linkage was created by C-2 epimerization of the initially introduced β-d-gluco-unit via DMSO/Ac2O oxidat

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