Cas 1401431-31-9,4,6-di-O-acetyl-2,3-di-O-benzyl-α-D-glucopyranosyl fluoride

1401431-31-9

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Basic information

Product Name: 4,6-di-O-acetyl-2,3-di-O-benzyl-α-D-glucopyranosyl fluoride
Synonyms: 4,6-di-O-acetyl-2,3-di-O-benzyl-α-D-glucopyranosyl fluoride
CAS NO:1401431-31-9
Molecular Formula:
Molecular Weight: 446.473
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: 4,6-di-O-acetyl-2,3-di-O-benzyl-α-D-glucopyranosyl fluoride(CAS DataBase Reference)
NIST Chemistry Reference: 4,6-di-O-acetyl-2,3-di-O-benzyl-α-D-glucopyranosyl fluoride(1401431-31-9)
EPA Substance Registry System: 4,6-di-O-acetyl-2,3-di-O-benzyl-α-D-glucopyranosyl fluoride(1401431-31-9)

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: 1401431-31-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1401431-31-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,1,4,3 and 1 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1401431-31:
(9*1)+(8*4)+(7*0)+(6*1)+(5*4)+(4*3)+(3*1)+(2*3)+(1*1)=89
89 % 10 = 9
So 1401431-31-9 is a valid CAS Registry Number.

1401431-31-9Upstream product

1225199-02-9 phenyl 4,6-di-O-acetyl-2,3-di-O-benzyl-1-thio-β-D-glucopyranoside

1401431-31-9Downstream Products

1401431-31-9Relevant academic research and scientific papers

A facile and convenient synthesis of disarmed glycosyl fluorides using in situ-generated iodine monofluoride (see Ref. 1)

Mugunthan,Kartha, K. P. Ravindranathan

, p. 5631 - 5634 (2012)

A facile and convenient synthesis of disarmed glycosyl fluorides using in situ-generated iodine monofluoride is reported. The method is tolerant to most of the popularly used protecting groups and gives exclusively the α-anomeric product in very good yields.

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