Cas 89615-27-0,(1S,2S,3S,4S)-3,4-Bis-(2-hydroxy-phenyl)-cyclobutane-1,2-dicarboxylic acid bis-[((S)-1-phenyl-ethyl)-amide]

89615-27-0

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Basic information

Product Name: (1S,2S,3S,4S)-3,4-Bis-(2-hydroxy-phenyl)-cyclobutane-1,2-dicarboxylic acid bis-[((S)-1-phenyl-ethyl)-amide]
Synonyms:
CAS NO:89615-27-0
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: (1S,2S,3S,4S)-3,4-Bis-(2-hydroxy-phenyl)-cyclobutane-1,2-dicarboxylic acid bis-[((S)-1-phenyl-ethyl)-amide](CAS DataBase Reference)
NIST Chemistry Reference: (1S,2S,3S,4S)-3,4-Bis-(2-hydroxy-phenyl)-cyclobutane-1,2-dicarboxylic acid bis-[((S)-1-phenyl-ethyl)-amide](89615-27-0)
EPA Substance Registry System: (1S,2S,3S,4S)-3,4-Bis-(2-hydroxy-phenyl)-cyclobutane-1,2-dicarboxylic acid bis-[((S)-1-phenyl-ethyl)-amide](89615-27-0)

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: 89615-27-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 89615-27-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,6,1 and 5 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 89615-27:
(7*8)+(6*9)+(5*6)+(4*1)+(3*5)+(2*2)+(1*7)=170
170 % 10 = 0
So 89615-27-0 is a valid CAS Registry Number.

89615-27-0Upstream product

89615-27-0Downstream Products

7734-65-8 t-3,c-4-bis(2-hydroxyphenyl)-r-1,t-2-cyclobutanedicarboxylic acid

89615-27-0Relevant 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 (1983)

(±)-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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