Cas 96016-13-6,1,6-Anhydro-2,4-di-O-benzyl-3-O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-β-D-galactopyranose

96016-13-6

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Basic information

Product Name: 1,6-Anhydro-2,4-di-O-benzyl-3-O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-β-D-galactopyranose
Synonyms: 1,6-Anhydro-2,4-di-O-benzyl-3-O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-β-D-galactopyranose
CAS NO:96016-13-6
Molecular Formula:
Molecular Weight: 672.683
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: 1,6-Anhydro-2,4-di-O-benzyl-3-O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-β-D-galactopyranose(CAS DataBase Reference)
NIST Chemistry Reference: 1,6-Anhydro-2,4-di-O-benzyl-3-O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-β-D-galactopyranose(96016-13-6)
EPA Substance Registry System: 1,6-Anhydro-2,4-di-O-benzyl-3-O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-β-D-galactopyranose(96016-13-6)

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: 96016-13-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 96016-13-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,0,1 and 6 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 96016-13:
(7*9)+(6*6)+(5*0)+(4*1)+(3*6)+(2*1)+(1*3)=126
126 % 10 = 6
So 96016-13-6 is a valid CAS Registry Number.

96016-13-6Upstream product

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96016-13-6Relevant academic research and scientific papers

LEWISSAEURE-KATALYSIERTE SYNTHESEN VON DI- UND TRI-SACCHARID-SEQUENZEN DER O- UND N-GLYCOPROTEINE, ANWENDUNG VON TRIMETHYLSILYLTRIFLUOROMETHANESULFONAT

Paulsen, Hans,Paal, Michael

, p. 53 - 70 (1984)

In the presence of trimethylsilyltrifluoromethanesulfonate as Lewis acid catalyst, β-acetates reacted, as glycosyl donors and with neighboring-group participation, with secondary hydroxyl groups of saccharides having low reactivity to give β-glycosidicall

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