Cas 1240591-08-5,ethyl 3,4,6-tri-O-benzyl-2-O-fluoren-9-ylmethoxycarbonyl-α-D-mannopyranosyl-(1->2)-3,4,6-tri-O-benzyl-1-thio-α-D-mannopyranoside

1240591-08-5

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Basic information

Product Name: ethyl 3,4,6-tri-O-benzyl-2-O-fluoren-9-ylmethoxycarbonyl-α-D-mannopyranosyl-(1->2)-3,4,6-tri-O-benzyl-1-thio-α-D-mannopyranoside
Synonyms:
CAS NO:1240591-08-5
Molecular Formula:
Molecular Weight: 1149.41
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: ethyl 3,4,6-tri-O-benzyl-2-O-fluoren-9-ylmethoxycarbonyl-α-D-mannopyranosyl-(1->2)-3,4,6-tri-O-benzyl-1-thio-α-D-mannopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: ethyl 3,4,6-tri-O-benzyl-2-O-fluoren-9-ylmethoxycarbonyl-α-D-mannopyranosyl-(1->2)-3,4,6-tri-O-benzyl-1-thio-α-D-mannopyranoside(1240591-08-5)
EPA Substance Registry System: ethyl 3,4,6-tri-O-benzyl-2-O-fluoren-9-ylmethoxycarbonyl-α-D-mannopyranosyl-(1->2)-3,4,6-tri-O-benzyl-1-thio-α-D-mannopyranoside(1240591-08-5)

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: 1240591-08-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1240591-08-5 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, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1240591-08:
(9*1)+(8*2)+(7*4)+(6*0)+(5*5)+(4*9)+(3*1)+(2*0)+(1*8)=125
125 % 10 = 5
So 1240591-08-5 is a valid CAS Registry Number.

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1240591-08-5Relevant 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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