Cas 735328-25-3,Acetic acid (2R,3S,4R,5S,6R)-5-acetoxy-6-acetoxymethyl-3-acetylamino-2-methyl-2-phenylselanyl-tetrahydro-pyran-4-yl ester

735328-25-3

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Basic information

Product Name: Acetic acid (2R,3S,4R,5S,6R)-5-acetoxy-6-acetoxymethyl-3-acetylamino-2-methyl-2-phenylselanyl-tetrahydro-pyran-4-yl ester
Synonyms:
CAS NO:735328-25-3
Molecular Formula:
Molecular Weight: 500.407
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 (2R,3S,4R,5S,6R)-5-acetoxy-6-acetoxymethyl-3-acetylamino-2-methyl-2-phenylselanyl-tetrahydro-pyran-4-yl ester(CAS DataBase Reference)
NIST Chemistry Reference: Acetic acid (2R,3S,4R,5S,6R)-5-acetoxy-6-acetoxymethyl-3-acetylamino-2-methyl-2-phenylselanyl-tetrahydro-pyran-4-yl ester(735328-25-3)
EPA Substance Registry System: Acetic acid (2R,3S,4R,5S,6R)-5-acetoxy-6-acetoxymethyl-3-acetylamino-2-methyl-2-phenylselanyl-tetrahydro-pyran-4-yl ester(735328-25-3)

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: 735328-25-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 735328-25-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,3,5,3,2 and 8 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 735328-25:
(8*7)+(7*3)+(6*5)+(5*3)+(4*2)+(3*8)+(2*2)+(1*5)=163
163 % 10 = 3
So 735328-25-3 is a valid CAS Registry Number.

735328-25-3Upstream product

108-24-7 acetic anhydride

735328-25-3Downstream Products

735328-25-3Relevant academic research and scientific papers

C-glycosides of 2-amino-2-deoxy sugars. β-C-glycosides and 1,1-disubstituted variants

Liu, Yan,Gallagher, Timothy

, p. 2445 - 2448 (2004)

(Equation Presented) C(1)-Substituted anomeric selenides, derived from azidoselenation of C(1)-methylated glycals, provide access to anomeric radical reactivity that has been used to generate β-C-glycosides and 1,1-disubstituted C-glycosides based on gala

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