Cas 247167-17-5,(2S,3R)-3-Hydroxy-2-[(2-nitro-benzenesulfonyl)-((2R,3R,4S,5R,6R)-3,4,5-triacetoxy-6-acetoxymethyl-tetrahydro-pyran-2-yl)-amino]-butyric acid

247167-17-5

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Basic information

Product Name: (2S,3R)-3-Hydroxy-2-[(2-nitro-benzenesulfonyl)-((2R,3R,4S,5R,6R)-3,4,5-triacetoxy-6-acetoxymethyl-tetrahydro-pyran-2-yl)-amino]-butyric acid
Synonyms: (2S,3R)-3-Hydroxy-2-[(2-nitro-benzenesulfonyl)-((2R,3R,4S,5R,6R)-3,4,5-triacetoxy-6-acetoxymethyl-tetrahydro-pyran-2-yl)-amino]-butyric acid
CAS NO:247167-17-5
Molecular Formula:
Molecular Weight: 634.572
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: (2S,3R)-3-Hydroxy-2-[(2-nitro-benzenesulfonyl)-((2R,3R,4S,5R,6R)-3,4,5-triacetoxy-6-acetoxymethyl-tetrahydro-pyran-2-yl)-amino]-butyric acid(CAS DataBase Reference)
NIST Chemistry Reference: (2S,3R)-3-Hydroxy-2-[(2-nitro-benzenesulfonyl)-((2R,3R,4S,5R,6R)-3,4,5-triacetoxy-6-acetoxymethyl-tetrahydro-pyran-2-yl)-amino]-butyric acid(247167-17-5)
EPA Substance Registry System: (2S,3R)-3-Hydroxy-2-[(2-nitro-benzenesulfonyl)-((2R,3R,4S,5R,6R)-3,4,5-triacetoxy-6-acetoxymethyl-tetrahydro-pyran-2-yl)-amino]-butyric acid(247167-17-5)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 247167-17-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 247167-17-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,7,1,6 and 7 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 247167-17:
(8*2)+(7*4)+(6*7)+(5*1)+(4*6)+(3*7)+(2*1)+(1*7)=145
145 % 10 = 5
So 247167-17-5 is a valid CAS Registry Number.

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247167-17-5Relevant academic research and scientific papers

Mitsunobu glycosylation of nitrobenzenesulfonamides: Novel route to Amadori rearrangement products

Turner, John J.,Wilschut, Niels,Overkleeft, Herman S.,Klaffke, Werner,Van der Marel, Gijs A.,Van Boom, Jacques H.

, p. 7039 - 7042 (1999)

Amino-acid derived 2-nitrobenzenesulfonamides were successfully condensed under Mitsunobu conditions with 2,3,4,6-tetra-O-acetyl-D-glucose to afford the fully protected glucosylamines in excellent yield. Upon total deprotection, these compounds rearranged to provide the corresponding Amadori products in good overall yield.

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