Cas 1309856-07-2,1-(3,4,6-tri-O-acetyl-2,5-anhydro-1-deoxy-D-glucitolyl)-4-(tert-butoxycarbonyl)-[1,2,3]-triazole

1309856-07-2

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Basic information

Product Name: 1-(3,4,6-tri-O-acetyl-2,5-anhydro-1-deoxy-D-glucitolyl)-4-(tert-butoxycarbonyl)-[1,2,3]-triazole
Synonyms: 1-(3,4,6-tri-O-acetyl-2,5-anhydro-1-deoxy-D-glucitolyl)-4-(tert-butoxycarbonyl)-[1,2,3]-triazole
CAS NO:1309856-07-2
Molecular Formula:
Molecular Weight: 441.438
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: 1-(3,4,6-tri-O-acetyl-2,5-anhydro-1-deoxy-D-glucitolyl)-4-(tert-butoxycarbonyl)-[1,2,3]-triazole(CAS DataBase Reference)
NIST Chemistry Reference: 1-(3,4,6-tri-O-acetyl-2,5-anhydro-1-deoxy-D-glucitolyl)-4-(tert-butoxycarbonyl)-[1,2,3]-triazole(1309856-07-2)
EPA Substance Registry System: 1-(3,4,6-tri-O-acetyl-2,5-anhydro-1-deoxy-D-glucitolyl)-4-(tert-butoxycarbonyl)-[1,2,3]-triazole(1309856-07-2)

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: 1309856-07-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1309856-07-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,0,9,8,5 and 6 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1309856-07:
(9*1)+(8*3)+(7*0)+(6*9)+(5*8)+(4*5)+(3*6)+(2*0)+(1*7)=172
172 % 10 = 2
So 1309856-07-2 is a valid CAS Registry Number.

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1309856-07-2Relevant academic research and scientific papers

An efficient approach to 2,5-anhydro-glucitol-based 1′-homo-N- nucleoside mimetics

Bhatt, Beenu,Thomson, Robin J.,Von Itzstein, Mark

, p. 2741 - 2743 (2011)

This Letter describes an efficient synthesis of a range of 1′-homo-N-nucleoside mimetics with a series of 4-substituted 1,2,3-triazoles replacing the natural nucleobase. The synthesis of 6-O-monosulfated 1′-homo-N-nucleoside mimetic derivatives is also discussed.

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