Cas 146236-92-2,3-{(R)-2-Methyl-5-oxo-3-[(R)-1-(2,4,6-trimethyl-phenyl)-ethoxy]-2,5-dihydro-furan-2-yl}-propionic acid ethyl ester

146236-92-2

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Basic information

Product Name: 3-{(R)-2-Methyl-5-oxo-3-[(R)-1-(2,4,6-trimethyl-phenyl)-ethoxy]-2,5-dihydro-furan-2-yl}-propionic acid ethyl ester
Synonyms:
CAS NO:146236-92-2
Molecular Formula:
Molecular Weight: 360.45
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: 3-{(R)-2-Methyl-5-oxo-3-[(R)-1-(2,4,6-trimethyl-phenyl)-ethoxy]-2,5-dihydro-furan-2-yl}-propionic acid ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 3-{(R)-2-Methyl-5-oxo-3-[(R)-1-(2,4,6-trimethyl-phenyl)-ethoxy]-2,5-dihydro-furan-2-yl}-propionic acid ethyl ester(146236-92-2)
EPA Substance Registry System: 3-{(R)-2-Methyl-5-oxo-3-[(R)-1-(2,4,6-trimethyl-phenyl)-ethoxy]-2,5-dihydro-furan-2-yl}-propionic acid ethyl ester(146236-92-2)

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: 146236-92-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 146236-92-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,6,2,3 and 6 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 146236-92:
(8*1)+(7*4)+(6*6)+(5*2)+(4*3)+(3*6)+(2*9)+(1*2)=132
132 % 10 = 2
So 146236-92-2 is a valid CAS Registry Number.

146236-92-2Upstream product

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146236-92-2Relevant academic research and scientific papers

A Convenient Stereoselective Synthesis of a (-)-Vertinolide Precursor

Datta, Apurba,Datta, Dinah,Schmidt, Richard R.

, p. 8035 - 8038 (2007/10/02)

A short practical method for the enantioselective synthesis of (-)-vertinolide precursor 2 is described.The readily available chiral β-alkoxy substituted acrylate 7 has been reacted with ethyl levulinate to form the tetronic acid nucleus 8, which in three subsequent steps was converted to the known precursor 2 in high overall yield.

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