Cas 109889-83-0,4-Bromo-benzoic acid (2R,3R,4S,5S,6S)-3-acetoxy-2-acetoxymethyl-6-methoxy-5-[(E)-3-(4-methoxy-phenyl)-acryloyloxy]-tetrahydro-pyran-4-yl ester

109889-83-0

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Basic information

Product Name: 4-Bromo-benzoic acid (2R,3R,4S,5S,6S)-3-acetoxy-2-acetoxymethyl-6-methoxy-5-[(E)-3-(4-methoxy-phenyl)-acryloyloxy]-tetrahydro-pyran-4-yl ester
Synonyms:
CAS NO:109889-83-0
Molecular Formula:
Molecular Weight: 621.436
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-Bromo-benzoic acid (2R,3R,4S,5S,6S)-3-acetoxy-2-acetoxymethyl-6-methoxy-5-[(E)-3-(4-methoxy-phenyl)-acryloyloxy]-tetrahydro-pyran-4-yl ester(CAS DataBase Reference)
NIST Chemistry Reference: 4-Bromo-benzoic acid (2R,3R,4S,5S,6S)-3-acetoxy-2-acetoxymethyl-6-methoxy-5-[(E)-3-(4-methoxy-phenyl)-acryloyloxy]-tetrahydro-pyran-4-yl ester(109889-83-0)
EPA Substance Registry System: 4-Bromo-benzoic acid (2R,3R,4S,5S,6S)-3-acetoxy-2-acetoxymethyl-6-methoxy-5-[(E)-3-(4-methoxy-phenyl)-acryloyloxy]-tetrahydro-pyran-4-yl ester(109889-83-0)

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: 109889-83-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 109889-83-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,8,8 and 9 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 109889-83:
(8*1)+(7*0)+(6*9)+(5*8)+(4*8)+(3*9)+(2*8)+(1*3)=180
180 % 10 = 0
So 109889-83-0 is a valid CAS Registry Number.

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109889-83-0Relevant academic research and scientific papers

Oligosaccharide microanalysis by c.d. spectroscopy. Reference curves for D-mannose derivatives.

Meyers,Ojika,Wiesler,Nakanishi

, p. 15 - 32 (2007/10/02)

This study completes the spectroscopic basis for a novel oligosaccharide microanalytical method, wherein a derivatization sequence provides monosaccharide subunits bearing two types of exciton-coupling chromophore groups ("bichromophoric") for circular di

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