Cas 866084-57-3,8-(methoxycarbonyl)octyl 2-O-(2,3,5-tri-O-benzoyl-α-D-arabinofuranosyl)-3,4,6-tri-O-benzyl-α-D-mannopyranoside

866084-57-3

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Basic information

Product Name: 8-(methoxycarbonyl)octyl 2-O-(2,3,5-tri-O-benzoyl-α-D-arabinofuranosyl)-3,4,6-tri-O-benzyl-α-D-mannopyranoside
Synonyms: 8-(methoxycarbonyl)octyl 2-O-(2,3,5-tri-O-benzoyl-α-D-arabinofuranosyl)-3,4,6-tri-O-benzyl-α-D-mannopyranoside
CAS NO:866084-57-3
Molecular Formula:
Molecular Weight: 1065.22
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: 8-(methoxycarbonyl)octyl 2-O-(2,3,5-tri-O-benzoyl-α-D-arabinofuranosyl)-3,4,6-tri-O-benzyl-α-D-mannopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: 8-(methoxycarbonyl)octyl 2-O-(2,3,5-tri-O-benzoyl-α-D-arabinofuranosyl)-3,4,6-tri-O-benzyl-α-D-mannopyranoside(866084-57-3)
EPA Substance Registry System: 8-(methoxycarbonyl)octyl 2-O-(2,3,5-tri-O-benzoyl-α-D-arabinofuranosyl)-3,4,6-tri-O-benzyl-α-D-mannopyranoside(866084-57-3)

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: 866084-57-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 866084-57-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,6,0,8 and 4 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 866084-57:
(8*8)+(7*6)+(6*6)+(5*0)+(4*8)+(3*4)+(2*5)+(1*7)=203
203 % 10 = 3
So 866084-57-3 is a valid CAS Registry Number.

866084-57-3Upstream product

866084-57-3Downstream Products

866084-57-3Relevant academic research and scientific papers

Synthesis of oligosaccharide fragments of the lipoarabinomannan from Rhodococcus ruber

Completo, Gladys C.,Ponto, Jessica A.,Lowary, Todd L.

, p. 517 - 527 (2005)

The synthesis of two oligosaccharide fragments (1 and 2) of the lipoarabinomannan from Rhodococcus ruber is reported. Thioglycoside donors were used to assemble these glycans, which were prepared as their 8-(methoxycarbonyl)octyl glycosides for potential

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