Cas 1240591-13-2,p-methoxyphenyl 3,4,6-tri-O-benzyl-2-O-fluoren-9-ylmethoxycarbonyl-β-D-mannopyranosyl-(1->2)-3,4,6-tri-O-benzyl-α-D-mannopyranoside

1240591-13-2

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Basic information

Product Name: p-methoxyphenyl 3,4,6-tri-O-benzyl-2-O-fluoren-9-ylmethoxycarbonyl-β-D-mannopyranosyl-(1->2)-3,4,6-tri-O-benzyl-α-D-mannopyranoside
Synonyms:
CAS NO:1240591-13-2
Molecular Formula:
Molecular Weight: 1211.42
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-methoxyphenyl 3,4,6-tri-O-benzyl-2-O-fluoren-9-ylmethoxycarbonyl-β-D-mannopyranosyl-(1->2)-3,4,6-tri-O-benzyl-α-D-mannopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: p-methoxyphenyl 3,4,6-tri-O-benzyl-2-O-fluoren-9-ylmethoxycarbonyl-β-D-mannopyranosyl-(1->2)-3,4,6-tri-O-benzyl-α-D-mannopyranoside(1240591-13-2)
EPA Substance Registry System: p-methoxyphenyl 3,4,6-tri-O-benzyl-2-O-fluoren-9-ylmethoxycarbonyl-β-D-mannopyranosyl-(1->2)-3,4,6-tri-O-benzyl-α-D-mannopyranoside(1240591-13-2)

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: 1240591-13-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1240591-13-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,0,5,9 and 1 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1240591-13:
(9*1)+(8*2)+(7*4)+(6*0)+(5*5)+(4*9)+(3*1)+(2*1)+(1*3)=122
122 % 10 = 2
So 1240591-13-2 is a valid CAS Registry Number.

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1240591-13-2Relevant academic research and scientific papers

Rapid assembly of gp120 oligosaccharide moieties via one-pot glycosidation-deprotection sequences

Pastore, Antonello,Adinolfi, Matteo,Iadonisi, Alfonso,Valerio, Silvia

experimental part, p. 1316 - 1323 (2010/10/02)

Mannosyl trihaloacetimidate donors equipped with a 2-O-Fmoc group can be effectively activated by catalytic Bi(OTf)3 in glycosidations. Despite the expected participating effect of the Fmoc group, the reaction solvent was found to be decisive f

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