Cas 676324-99-5,acetamidyl-6-deoxy-3,4-di-O-acetyl-2-O-benzyl-L-galactopyranose N-phenyl trifluoroacetimidate

676324-99-5

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Basic information

Product Name: acetamidyl-6-deoxy-3,4-di-O-acetyl-2-O-benzyl-L-galactopyranose N-phenyl trifluoroacetimidate
Synonyms: acetamidyl-6-deoxy-3,4-di-O-acetyl-2-O-benzyl-L-galactopyranose N-phenyl trifluoroacetimidate
CAS NO:676324-99-5
Molecular Formula:
Molecular Weight: 509.479
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: acetamidyl-6-deoxy-3,4-di-O-acetyl-2-O-benzyl-L-galactopyranose N-phenyl trifluoroacetimidate(CAS DataBase Reference)
NIST Chemistry Reference: acetamidyl-6-deoxy-3,4-di-O-acetyl-2-O-benzyl-L-galactopyranose N-phenyl trifluoroacetimidate(676324-99-5)
EPA Substance Registry System: acetamidyl-6-deoxy-3,4-di-O-acetyl-2-O-benzyl-L-galactopyranose N-phenyl trifluoroacetimidate(676324-99-5)

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: 676324-99-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 676324-99-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,7,6,3,2 and 4 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 676324-99:
(8*6)+(7*7)+(6*6)+(5*3)+(4*2)+(3*4)+(2*9)+(1*9)=195
195 % 10 = 5
So 676324-99-5 is a valid CAS Registry Number.

676324-99-5Upstream product

676324-99-5Downstream Products

676324-99-5Relevant academic research and scientific papers

Synthesis of a sialic acid α(2-3) galactose building block and its use in a linear synthesis of sialyl Lewis X

Hanashima, Shinya,Castagner, Bastien,Esposito, Davide,Nokami, Toshiki,Seeberger, Peter H.

, p. 1777 - 1779 (2007)

The ubiquity of the sialic acid α(2-3) galactose linkage in oligosaccharides of biological relevance necessitates a building block for the incorporation of this motif into oligosaccharides prepared by modular synthesis. The linear synthesis of the sialyl

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