Cas 189622-68-2,methyl 2,4-di-O-benzoyl-3-O-benzyl-6-O-chloroacetyl-β-D-galactopyranosyl-(1->4)-2,3,6-tri-O-benzoyl-α-D-mannopyranoside

189622-68-2

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Basic information

Product Name: methyl 2,4-di-O-benzoyl-3-O-benzyl-6-O-chloroacetyl-β-D-galactopyranosyl-(1->4)-2,3,6-tri-O-benzoyl-α-D-mannopyranoside
Synonyms: methyl 2,4-di-O-benzoyl-3-O-benzyl-6-O-chloroacetyl-β-D-galactopyranosyl-(1->4)-2,3,6-tri-O-benzoyl-α-D-mannopyranoside
CAS NO:189622-68-2
Molecular Formula:
Molecular Weight: 1043.47
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: methyl 2,4-di-O-benzoyl-3-O-benzyl-6-O-chloroacetyl-β-D-galactopyranosyl-(1->4)-2,3,6-tri-O-benzoyl-α-D-mannopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: methyl 2,4-di-O-benzoyl-3-O-benzyl-6-O-chloroacetyl-β-D-galactopyranosyl-(1->4)-2,3,6-tri-O-benzoyl-α-D-mannopyranoside(189622-68-2)
EPA Substance Registry System: methyl 2,4-di-O-benzoyl-3-O-benzyl-6-O-chloroacetyl-β-D-galactopyranosyl-(1->4)-2,3,6-tri-O-benzoyl-α-D-mannopyranoside(189622-68-2)

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: 189622-68-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 189622-68-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,9,6,2 and 2 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 189622-68:
(8*1)+(7*8)+(6*9)+(5*6)+(4*2)+(3*2)+(2*6)+(1*8)=182
182 % 10 = 2
So 189622-68-2 is a valid CAS Registry Number.

189622-68-2Upstream product

189622-68-2Downstream Products

189622-72-8 methyl 2,4-di-O-benzoyl-6-O-chloroacetyl-β-D-galactopyranosyl-(1->4)-2,3,6-tri-O-benzoyl-α-D-mannopyranoside

189622-68-2Relevant academic research and scientific papers

Parasite glycoconjugates. Part 6. Chemical synthesis of phosphorylated penta- and hepta-saccharide fragments of Leishmania major antigenic lipophosphoglycan

Nikolaev, Andrei V.,Watt, Gregory M.,Ferguson, Michael A. J.,Brimacombe, John S.

, p. 969 - 979 (2007/10/03)

The phosphorylated branched oligosaccharides 1 and 2, fragments of the phosphoglycan portion of Leishmania major lipophosphoglycan, have been synthesized using the trichloroacetimidate method for the glycosylation reactions and the phosphoramidite and hydrogenphosphonate methods for phosphorylation.

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