Cas 757242-11-8,(S)-2-[(2-Nitro-benzenesulfonyl)-((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-hydroxymethyl-tetrahydro-pyran-2-yl)-amino]-3-phenyl-propionic acid

757242-11-8

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Basic information

Product Name: (S)-2-[(2-Nitro-benzenesulfonyl)-((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-hydroxymethyl-tetrahydro-pyran-2-yl)-amino]-3-phenyl-propionic acid
Synonyms: (S)-2-[(2-Nitro-benzenesulfonyl)-((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-hydroxymethyl-tetrahydro-pyran-2-yl)-amino]-3-phenyl-propionic acid
CAS NO:757242-11-8
Molecular Formula:
Molecular Weight: 512.494
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: (S)-2-[(2-Nitro-benzenesulfonyl)-((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-hydroxymethyl-tetrahydro-pyran-2-yl)-amino]-3-phenyl-propionic acid(CAS DataBase Reference)
NIST Chemistry Reference: (S)-2-[(2-Nitro-benzenesulfonyl)-((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-hydroxymethyl-tetrahydro-pyran-2-yl)-amino]-3-phenyl-propionic acid(757242-11-8)
EPA Substance Registry System: (S)-2-[(2-Nitro-benzenesulfonyl)-((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-hydroxymethyl-tetrahydro-pyran-2-yl)-amino]-3-phenyl-propionic acid(757242-11-8)

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: 757242-11-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 757242-11-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,5,7,2,4 and 2 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 757242-11:
(8*7)+(7*5)+(6*7)+(5*2)+(4*4)+(3*2)+(2*1)+(1*1)=168
168 % 10 = 8
So 757242-11-8 is a valid CAS Registry Number.

757242-11-8Upstream product

757242-11-8Downstream Products

86334-92-1 N-(1-deoxy-D-fructos-1-yl)-L-phenylalanine

757242-11-8Relevant 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 (2007/10/03)

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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