Cas 226252-64-8,(R)-2-Propyl-piperidine-1-carboxylic acid (1S,2R,5S)-2-isopropyl-5-methyl-cyclohexyl ester

226252-64-8

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Basic information

Product Name: (R)-2-Propyl-piperidine-1-carboxylic acid (1S,2R,5S)-2-isopropyl-5-methyl-cyclohexyl ester
Synonyms: (R)-2-Propyl-piperidine-1-carboxylic acid (1S,2R,5S)-2-isopropyl-5-methyl-cyclohexyl ester
CAS NO:226252-64-8
Molecular Formula:
Molecular Weight: 309.492
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: (R)-2-Propyl-piperidine-1-carboxylic acid (1S,2R,5S)-2-isopropyl-5-methyl-cyclohexyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (R)-2-Propyl-piperidine-1-carboxylic acid (1S,2R,5S)-2-isopropyl-5-methyl-cyclohexyl ester(226252-64-8)
EPA Substance Registry System: (R)-2-Propyl-piperidine-1-carboxylic acid (1S,2R,5S)-2-isopropyl-5-methyl-cyclohexyl ester(226252-64-8)

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: 226252-64-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 226252-64-8 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, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 226252-64:
(8*2)+(7*2)+(6*6)+(5*2)+(4*5)+(3*2)+(2*6)+(1*4)=118
118 % 10 = 8
So 226252-64-8 is a valid CAS Registry Number.

226252-64-8Upstream product

226252-64-8Downstream Products

6032-02-6 (-)-N-methylconiine

226252-64-8Relevant 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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