Cas 906338-80-5,Acetic acid (2S,3R,3aS,6S,6aS)-6-acetoxy-2-(4-nitro-phenoxy)-5-oxo-hexahydro-furo[3,2-b]furan-3-yl ester

906338-80-5

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Basic information

Product Name: Acetic acid (2S,3R,3aS,6S,6aS)-6-acetoxy-2-(4-nitro-phenoxy)-5-oxo-hexahydro-furo[3,2-b]furan-3-yl ester
Synonyms:
CAS NO:906338-80-5
Molecular Formula:
Molecular Weight: 381.296
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: Acetic acid (2S,3R,3aS,6S,6aS)-6-acetoxy-2-(4-nitro-phenoxy)-5-oxo-hexahydro-furo[3,2-b]furan-3-yl ester(CAS DataBase Reference)
NIST Chemistry Reference: Acetic acid (2S,3R,3aS,6S,6aS)-6-acetoxy-2-(4-nitro-phenoxy)-5-oxo-hexahydro-furo[3,2-b]furan-3-yl ester(906338-80-5)
EPA Substance Registry System: Acetic acid (2S,3R,3aS,6S,6aS)-6-acetoxy-2-(4-nitro-phenoxy)-5-oxo-hexahydro-furo[3,2-b]furan-3-yl ester(906338-80-5)

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: 906338-80-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 906338-80-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,6,3,3 and 8 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 906338-80:
(8*9)+(7*0)+(6*6)+(5*3)+(4*3)+(3*8)+(2*8)+(1*0)=175
175 % 10 = 5
So 906338-80-5 is a valid CAS Registry Number.

906338-80-5Upstream product

63-29-6 D-glucurono-6,3-lactone

906338-80-5Downstream Products

906338-80-5Relevant academic research and scientific papers

p-nitrophenyl β-D-glucopyranosiduronic analogs as potential substrates for β-glucuronidase

Azoulay, Michel,Ivastchenko, Nadia,Florent, Jean-Claude,Monneret, Claude

, p. 1307 - 1310 (1997)

Three p-nitrophenyl-β-D)-glycosides including gluco-hex-4-enopyranosiduronic, glucofuranosiduronic and xylofuranosiduronic moieties have been prepared. None of them appeared to be a better substrate far β-glucuronidase from bovine origin than usual p-nitrophenyl-β-D-glucuronide.

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