Cas 115346-83-3,Benzoic acid (R)-3-[(1R,2S,5R)-2-isopropyl-5-methyl-1-(2-oxo-2-phenyl-ethyl)-cyclohexyloxy]-1-phenethyl-propyl ester

115346-83-3

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Basic information

Product Name: Benzoic acid (R)-3-[(1R,2S,5R)-2-isopropyl-5-methyl-1-(2-oxo-2-phenyl-ethyl)-cyclohexyloxy]-1-phenethyl-propyl ester
Synonyms:
CAS NO:115346-83-3
Molecular Formula:
Molecular Weight: 540.743
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: Benzoic acid (R)-3-[(1R,2S,5R)-2-isopropyl-5-methyl-1-(2-oxo-2-phenyl-ethyl)-cyclohexyloxy]-1-phenethyl-propyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Benzoic acid (R)-3-[(1R,2S,5R)-2-isopropyl-5-methyl-1-(2-oxo-2-phenyl-ethyl)-cyclohexyloxy]-1-phenethyl-propyl ester(115346-83-3)
EPA Substance Registry System: Benzoic acid (R)-3-[(1R,2S,5R)-2-isopropyl-5-methyl-1-(2-oxo-2-phenyl-ethyl)-cyclohexyloxy]-1-phenethyl-propyl ester(115346-83-3)

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: 115346-83-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 115346-83-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,3,4 and 6 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 115346-83:
(8*1)+(7*1)+(6*5)+(5*3)+(4*4)+(3*6)+(2*8)+(1*3)=113
113 % 10 = 3
So 115346-83-3 is a valid CAS Registry Number.

115346-83-3Upstream product

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115346-83-3Relevant academic research and scientific papers

AN ENANTIODIFFERENTIATING CONVERSION OF RACEMIC 1,3-ALKANEDIOLS INTO ENANTIOMERICALLY PURE MATERIALS

Harada, Toshiro,Kurokawa, Hideaki,Oku, Akira

, p. 4847 - 4848 (2007/10/02)

Titanium tetrachloride promoted ring-cleavage reaction of a mixture of diastereomeric spiroketals derived from racemic 1,3-alkanediols and l-menthone, followed by benzoylation by Mitsunobu reaction, and the subsequent hydrolysis gave enantiomerically pure 1,3-alkanediols.

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