Cas 1259987-77-3,pent-4-en-1-yl (2-deoxy-3,4,6-tri-O-benzyl-β-D-glucopyranosyl)-(1->2)-3,4,6-tri-O-benzyl-α-D-glucopyranoside

1259987-77-3

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Basic information

Product Name: pent-4-en-1-yl (2-deoxy-3,4,6-tri-O-benzyl-β-D-glucopyranosyl)-(1->2)-3,4,6-tri-O-benzyl-α-D-glucopyranoside
Synonyms:
CAS NO:1259987-77-3
Molecular Formula:
Molecular Weight: 935.167
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: pent-4-en-1-yl (2-deoxy-3,4,6-tri-O-benzyl-β-D-glucopyranosyl)-(1->2)-3,4,6-tri-O-benzyl-α-D-glucopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: pent-4-en-1-yl (2-deoxy-3,4,6-tri-O-benzyl-β-D-glucopyranosyl)-(1->2)-3,4,6-tri-O-benzyl-α-D-glucopyranoside(1259987-77-3)
EPA Substance Registry System: pent-4-en-1-yl (2-deoxy-3,4,6-tri-O-benzyl-β-D-glucopyranosyl)-(1->2)-3,4,6-tri-O-benzyl-α-D-glucopyranoside(1259987-77-3)

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: 1259987-77-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1259987-77-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,9,9,8 and 7 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1259987-77:
(9*1)+(8*2)+(7*5)+(6*9)+(5*9)+(4*8)+(3*7)+(2*7)+(1*7)=233
233 % 10 = 3
So 1259987-77-3 is a valid CAS Registry Number.

1259987-77-3Upstream product

130781-26-9 4-Pentenyl 3,4,6-tri-O-benzyl-β-D-glucopyranoside

1259987-77-3Downstream Products

1259987-77-3Relevant academic research and scientific papers

Fluorine-directed glycosylation

Bucher, Christoph,Gilmour, Ryan

supporting information; experimental part, p. 8724 - 8728 (2011/01/06)

Everything's under control: A stabilizing fluorine electrostatic interaction has been exploited to control oxonium ion conformation in 2-fluoropyranose derivatives (see scheme). When matched with the inductive nature of the protecting groups, the glycosyl

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