Cas 220148-70-9,Acetic acid (2R,3S,4R,5R,6R)-5-azido-4-benzyloxy-2-benzyloxymethyl-6-(1-methyl-allyloxy)-tetrahydro-pyran-3-yl ester

220148-70-9

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Basic information

Product Name: Acetic acid (2R,3S,4R,5R,6R)-5-azido-4-benzyloxy-2-benzyloxymethyl-6-(1-methyl-allyloxy)-tetrahydro-pyran-3-yl ester
Synonyms:
CAS NO:220148-70-9
Molecular Formula:
Molecular Weight: 481.549
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: Acetic acid (2R,3S,4R,5R,6R)-5-azido-4-benzyloxy-2-benzyloxymethyl-6-(1-methyl-allyloxy)-tetrahydro-pyran-3-yl ester(CAS DataBase Reference)
NIST Chemistry Reference: Acetic acid (2R,3S,4R,5R,6R)-5-azido-4-benzyloxy-2-benzyloxymethyl-6-(1-methyl-allyloxy)-tetrahydro-pyran-3-yl ester(220148-70-9)
EPA Substance Registry System: Acetic acid (2R,3S,4R,5R,6R)-5-azido-4-benzyloxy-2-benzyloxymethyl-6-(1-methyl-allyloxy)-tetrahydro-pyran-3-yl ester(220148-70-9)

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: 220148-70-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 220148-70-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,0,1,4 and 8 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 220148-70:
(8*2)+(7*2)+(6*0)+(5*1)+(4*4)+(3*8)+(2*7)+(1*0)=89
89 % 10 = 9
So 220148-70-9 is a valid CAS Registry Number.

220148-70-9Upstream product

220148-70-9Downstream Products

220148-70-9Relevant academic research and scientific papers

Vinyl glycosides in oligosaccharide synthesis (part 5)1: A latent- active glycosylation strategy for the preparation of branched trisaccharide libraries

Johnson, Matthew,Arles, Christele,Boons, Geert-Jan

, p. 9801 - 9804 (2007/10/03)

For the first time, an efficient strategy is described for the preparation of orthogonally protected branched and linear saccharide libraries which can be further functionalised. A small number of key building blocks can be converted into a wide range of glycosyl donors and acceptors.

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