Cas 115216-35-8,benzyl 3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl-(1->3)-2,6-di-O-benzyl-β-D-galactopyranoside

115216-35-8

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Basic information

Product Name: benzyl 3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl-(1->3)-2,6-di-O-benzyl-β-D-galactopyranoside
Synonyms:
CAS NO:115216-35-8
Molecular Formula:
Molecular Weight: 867.904
EINECS: N/A
Product Categories: N/A
Mol File: 115216-35-8.mol
Article Data: 2

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: benzyl 3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl-(1->3)-2,6-di-O-benzyl-β-D-galactopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: benzyl 3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl-(1->3)-2,6-di-O-benzyl-β-D-galactopyranoside(115216-35-8)
EPA Substance Registry System: benzyl 3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl-(1->3)-2,6-di-O-benzyl-β-D-galactopyranoside(115216-35-8)

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: 115216-35-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 115216-35-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,2,1 and 6 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 115216-35:
(8*1)+(7*1)+(6*5)+(5*2)+(4*1)+(3*6)+(2*3)+(1*5)=88
88 % 10 = 8
So 115216-35-8 is a valid CAS Registry Number.

115216-35-8Upstream product

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115216-35-8Relevant articles and documents

Glycosyl sulfonium ions as storable intermediates for glycosylations

Nokami, Toshiki,Nozaki, Yuki,Saigusa, Yoshihiro,Shibuya, Akito,Manabe, Shino,Ito, Yukishige,Yoshida, Jun-Ichi

, p. 1544 - 1547 (2011)

Glycosyl sulfonium ions, which serve as persistent glycosyl cation equivalents, were prepared by the addition of diorganosulfides to an electrochemically generated glycosyl triflate. Low-temperature and variable-temperature NMR studies were performed to r

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