Cas 1190718-86-5,p-methoxybenzyl (2-acetamido-4-O-allyl-3,6-di-O-benzyl-2-deoxy-β-D-mannopyranosyl)-(1->4)-(2,3,6-tri-O-benzyl-α-D-glucopyranosyl)-(1->3)-2,4-di-O-benzyl-α-L-rhamnopyranoside

1190718-86-5

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Basic information

Product Name: p-methoxybenzyl (2-acetamido-4-O-allyl-3,6-di-O-benzyl-2-deoxy-β-D-mannopyranosyl)-(1->4)-(2,3,6-tri-O-benzyl-α-D-glucopyranosyl)-(1->3)-2,4-di-O-benzyl-α-L-rhamnopyranoside
Synonyms:
CAS NO:1190718-86-5
Molecular Formula:
Molecular Weight: 1320.58
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: p-methoxybenzyl (2-acetamido-4-O-allyl-3,6-di-O-benzyl-2-deoxy-β-D-mannopyranosyl)-(1->4)-(2,3,6-tri-O-benzyl-α-D-glucopyranosyl)-(1->3)-2,4-di-O-benzyl-α-L-rhamnopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: p-methoxybenzyl (2-acetamido-4-O-allyl-3,6-di-O-benzyl-2-deoxy-β-D-mannopyranosyl)-(1->4)-(2,3,6-tri-O-benzyl-α-D-glucopyranosyl)-(1->3)-2,4-di-O-benzyl-α-L-rhamnopyranoside(1190718-86-5)
EPA Substance Registry System: p-methoxybenzyl (2-acetamido-4-O-allyl-3,6-di-O-benzyl-2-deoxy-β-D-mannopyranosyl)-(1->4)-(2,3,6-tri-O-benzyl-α-D-glucopyranosyl)-(1->3)-2,4-di-O-benzyl-α-L-rhamnopyranoside(1190718-86-5)

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: 1190718-86-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1190718-86-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,0,7,1 and 8 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1190718-86:
(9*1)+(8*1)+(7*9)+(6*0)+(5*7)+(4*1)+(3*8)+(2*8)+(1*6)=165
165 % 10 = 5
So 1190718-86-5 is a valid CAS Registry Number.

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1190718-86-5Relevant academic research and scientific papers

A new route for the synthesis of Streptococcus pneumoniae 19F and 19A capsular polysaccharide fragments avoiding the β-mannosamine glycosylation step

Bonaccorsi, Filippo,Catelani, Giorgio,Oscarson, Stefan

, p. 1442 - 1448 (2009)

The recently described [Attolino, E.; Bonaccorsi, F.; Catelani, G.; D'Andrea, F. Carbohydr. Res. 2008, 343, 2545-2556.] β-d-MaNAcp-(1→4)-β-d-Glcp thiophenyl glycosyl donor 3 was used in α-glycosylation reactions of OH-2 and OH-3 of the suitably protected

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