Cas 915378-91-5,Propanoic acid, 2,2-dimethyl-, (2S,3R)-2-cyclohexyl-3,4-dihydro-4-oxo-2H-pyran-3-yl ester

915378-91-5

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Basic information

Product Name: Propanoic acid, 2,2-dimethyl-, (2S,3R)-2-cyclohexyl-3,4-dihydro-4-oxo-2H-pyran-3-yl ester
Synonyms:
CAS NO:915378-91-5
Molecular Formula: C16H24O4
Molecular Weight: 280.364
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: Propanoic acid, 2,2-dimethyl-, (2S,3R)-2-cyclohexyl-3,4-dihydro-4-oxo-2H-pyran-3-yl ester(CAS DataBase Reference)
NIST Chemistry Reference: Propanoic acid, 2,2-dimethyl-, (2S,3R)-2-cyclohexyl-3,4-dihydro-4-oxo-2H-pyran-3-yl ester(915378-91-5)
EPA Substance Registry System: Propanoic acid, 2,2-dimethyl-, (2S,3R)-2-cyclohexyl-3,4-dihydro-4-oxo-2H-pyran-3-yl ester(915378-91-5)

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: 915378-91-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 915378-91-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,5,3,7 and 8 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 915378-91:
(8*9)+(7*1)+(6*5)+(5*3)+(4*7)+(3*8)+(2*9)+(1*1)=195
195 % 10 = 5
So 915378-91-5 is a valid CAS Registry Number.

915378-91-5Upstream product

915378-91-5Downstream Products

145624-56-2 (-)-(S)-2-cyclohexyl-2,3-dihydro-4H-pyran-4-one

915378-91-5Relevant academic research and scientific papers

Pyrones to pyrans: Enantioselective radical additions to acyloxy pyrones

Sibi, Mukund P.,Zimmerman, Jake

, p. 13346 - 13347 (2006)

This paper describes a highly site-, diastereo-, and enantioselective intermolecular radical addition/hydrogen atom transfer to hydroxypyrone pyromeconic and kojic acids. The methodology can be extended to the formation of chiral quaternary centers. The p

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