Cas 244258-58-0,(5R,6R,7S,8R)-N-{6,7,8-Tris(benzyloxy)-5-[(benzyloxy)methyl]-5,6,7,8-tetrahydroimidazo[1,2-a]pyridin-3-yl}acetamide

244258-58-0

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Basic information

Product Name: (5R,6R,7S,8R)-N-{6,7,8-Tris(benzyloxy)-5-[(benzyloxy)methyl]-5,6,7,8-tetrahydroimidazo[1,2-a]pyridin-3-yl}acetamide
Synonyms:
CAS NO:244258-58-0
Molecular Formula:
Molecular Weight: 617.745
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: (5R,6R,7S,8R)-N-{6,7,8-Tris(benzyloxy)-5-[(benzyloxy)methyl]-5,6,7,8-tetrahydroimidazo[1,2-a]pyridin-3-yl}acetamide(CAS DataBase Reference)
NIST Chemistry Reference: (5R,6R,7S,8R)-N-{6,7,8-Tris(benzyloxy)-5-[(benzyloxy)methyl]-5,6,7,8-tetrahydroimidazo[1,2-a]pyridin-3-yl}acetamide(244258-58-0)
EPA Substance Registry System: (5R,6R,7S,8R)-N-{6,7,8-Tris(benzyloxy)-5-[(benzyloxy)methyl]-5,6,7,8-tetrahydroimidazo[1,2-a]pyridin-3-yl}acetamide(244258-58-0)

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: 244258-58-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 244258-58-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,4,2,5 and 8 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 244258-58:
(8*2)+(7*4)+(6*4)+(5*2)+(4*5)+(3*8)+(2*5)+(1*8)=140
140 % 10 = 0
So 244258-58-0 is a valid CAS Registry Number.

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244258-58-0Relevant academic research and scientific papers

Synthesis of glucose- and mannose-derived N-acetylamino imidazopyridines and their evaluation as inhibitors of glycosidases

Panday, Narendra,Vasella, Andrea

, p. 1459 - 1468 (2007/10/03)

The correlation between basicity and inhibitory power of tetrahydropyridoazole type glycosidase inhibitors has been used to determine the effect of substituents at positions 2 and 3. The gluco-and manno- configurated 2-acetamido derivatives 11 and 13 were

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