Cas 219829-92-2,N-[(2R,3R,4R,5S,6R)-4,5-Bis-benzyloxy-6-benzyloxymethyl-2-(pyridine-2-sulfonyl)-tetrahydro-pyran-3-yl]-acetamide

219829-92-2

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Basic information

Product Name: N-[(2R,3R,4R,5S,6R)-4,5-Bis-benzyloxy-6-benzyloxymethyl-2-(pyridine-2-sulfonyl)-tetrahydro-pyran-3-yl]-acetamide
Synonyms:
CAS NO:219829-92-2
Molecular Formula:
Molecular Weight: 616.735
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: N-[(2R,3R,4R,5S,6R)-4,5-Bis-benzyloxy-6-benzyloxymethyl-2-(pyridine-2-sulfonyl)-tetrahydro-pyran-3-yl]-acetamide(CAS DataBase Reference)
NIST Chemistry Reference: N-[(2R,3R,4R,5S,6R)-4,5-Bis-benzyloxy-6-benzyloxymethyl-2-(pyridine-2-sulfonyl)-tetrahydro-pyran-3-yl]-acetamide(219829-92-2)
EPA Substance Registry System: N-[(2R,3R,4R,5S,6R)-4,5-Bis-benzyloxy-6-benzyloxymethyl-2-(pyridine-2-sulfonyl)-tetrahydro-pyran-3-yl]-acetamide(219829-92-2)

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: 219829-92-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 219829-92-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,9,8,2 and 9 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 219829-92:
(8*2)+(7*1)+(6*9)+(5*8)+(4*2)+(3*9)+(2*9)+(1*2)=172
172 % 10 = 2
So 219829-92-2 is a valid CAS Registry Number.

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219829-92-2Relevant academic research and scientific papers

Stereoselective synthesis of α-C-glucosamines via anomeric organosamarium reagents

Andersen, Lise,Mikkelsen, Lise Munch,Beau, Jean-Marie,Skrydstrup, Troels

, p. 1393 - 1395 (2007/10/03)

The direct coupling of the pyridyl sulfone of N-acetylglucosamine with aldehydes or ketones is promoted by samarium diiodide affording the corresponding α-C-glycosides preferentially. A C-disaccharide has been synthesized using this approach.

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