Cas 226252-52-4,4-Oxo-5,6-dihydro-4H-pyridine-1,3-dicarboxylic acid 1-((1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl) ester 3-((1S,2R,5S)-2-isopropyl-5-methyl-cyclohexyl) ester

226252-52-4

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Basic information

Product Name: 4-Oxo-5,6-dihydro-4H-pyridine-1,3-dicarboxylic acid 1-((1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl) ester 3-((1S,2R,5S)-2-isopropyl-5-methyl-cyclohexyl) ester
Synonyms:
CAS NO:226252-52-4
Molecular Formula:
Molecular Weight: 461.642
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: 4-Oxo-5,6-dihydro-4H-pyridine-1,3-dicarboxylic acid 1-((1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl) ester 3-((1S,2R,5S)-2-isopropyl-5-methyl-cyclohexyl) ester(CAS DataBase Reference)
NIST Chemistry Reference: 4-Oxo-5,6-dihydro-4H-pyridine-1,3-dicarboxylic acid 1-((1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl) ester 3-((1S,2R,5S)-2-isopropyl-5-methyl-cyclohexyl) ester(226252-52-4)
EPA Substance Registry System: 4-Oxo-5,6-dihydro-4H-pyridine-1,3-dicarboxylic acid 1-((1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl) ester 3-((1S,2R,5S)-2-isopropyl-5-methyl-cyclohexyl) ester(226252-52-4)

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: 226252-52-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 226252-52-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,6,2,5 and 2 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 226252-52:
(8*2)+(7*2)+(6*6)+(5*2)+(4*5)+(3*2)+(2*5)+(1*2)=114
114 % 10 = 4
So 226252-52-4 is a valid CAS Registry Number.

226252-52-4Upstream product

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226252-52-4Relevant academic research and scientific papers

Lewis acid mediated diastereoselective allylation of 3- menthyloxycarbonyl-5,6-dihydropyridin-4-ones

Brocherieux-Lanoy, Sylvie,Dhimane, Hamid,Vanucci-Bacqué, Corinne,Lhommet, Gérard

, p. 405 - 408 (2007/10/03)

Sakurai allylation of menthyl enoates 5a-c afforded adducts 7a-c with low to excellent facial selectivity, depending on the Lewis acid employed to promote this 1,4-nucleophilic addition of allyltrimethylsilane. A chelated model was assumed to explain the

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