Cas 89537-65-5,(1R,2R,3R,4R)-3,4-Bis-(2-hydroxy-phenyl)-cyclobutane-1,2-dicarboxylic acid bis-[((S)-1-phenyl-ethyl)-amide]

89537-65-5

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Basic information

Product Name: (1R,2R,3R,4R)-3,4-Bis-(2-hydroxy-phenyl)-cyclobutane-1,2-dicarboxylic acid bis-[((S)-1-phenyl-ethyl)-amide]
Synonyms:
CAS NO:89537-65-5
Molecular Formula:
Molecular Weight: 534.655
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: (1R,2R,3R,4R)-3,4-Bis-(2-hydroxy-phenyl)-cyclobutane-1,2-dicarboxylic acid bis-[((S)-1-phenyl-ethyl)-amide](CAS DataBase Reference)
NIST Chemistry Reference: (1R,2R,3R,4R)-3,4-Bis-(2-hydroxy-phenyl)-cyclobutane-1,2-dicarboxylic acid bis-[((S)-1-phenyl-ethyl)-amide](89537-65-5)
EPA Substance Registry System: (1R,2R,3R,4R)-3,4-Bis-(2-hydroxy-phenyl)-cyclobutane-1,2-dicarboxylic acid bis-[((S)-1-phenyl-ethyl)-amide](89537-65-5)

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: 89537-65-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 89537-65-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,5,3 and 7 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 89537-65:
(7*8)+(6*9)+(5*5)+(4*3)+(3*7)+(2*6)+(1*5)=185
185 % 10 = 5
So 89537-65-5 is a valid CAS Registry Number.

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89537-65-5Relevant academic research and scientific papers

Optical resolution of anti head-to-head coumarin dimer and determination of its absolute configuration based on CD spectral data

Saigo,Sekimoto,Yonezawa,Hasegawa

, p. 5381 - 5384 (2007/10/02)

(±)-anti Head-to-head coumarin dimer was successfully resolved into a pair of optically active forms in high yields, of which the absolute configuration was determined on the basis of CD and 1H-NMR spectral data.

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