Cas 365540-16-5,(R)-2-[(R)-1-((S)-1-Phenyl-ethyl)-piperidin-2-yl]-pentane-1,5-diol

365540-16-5

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Basic information

Product Name: (R)-2-[(R)-1-((S)-1-Phenyl-ethyl)-piperidin-2-yl]-pentane-1,5-diol
Synonyms: (R)-2-[(R)-1-((S)-1-Phenyl-ethyl)-piperidin-2-yl]-pentane-1,5-diol
CAS NO:365540-16-5
Molecular Formula:
Molecular Weight: 291.434
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-[(R)-1-((S)-1-Phenyl-ethyl)-piperidin-2-yl]-pentane-1,5-diol(CAS DataBase Reference)
NIST Chemistry Reference: (R)-2-[(R)-1-((S)-1-Phenyl-ethyl)-piperidin-2-yl]-pentane-1,5-diol(365540-16-5)
EPA Substance Registry System: (R)-2-[(R)-1-((S)-1-Phenyl-ethyl)-piperidin-2-yl]-pentane-1,5-diol(365540-16-5)

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: 365540-16-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 365540-16-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,6,5,5,4 and 0 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 365540-16:
(8*3)+(7*6)+(6*5)+(5*5)+(4*4)+(3*0)+(2*1)+(1*6)=145
145 % 10 = 5
So 365540-16-5 is a valid CAS Registry Number.

365540-16-5Upstream product

254428-02-9 (R)-2-[(R)-1-((S)-1-Phenyl-ethyl)-piperidin-2-yl]-pent-4-enoic acid ethyl ester

365540-16-5Downstream Products

486-70-4 lupinine

365540-16-5Relevant academic research and scientific papers

Syntheses from chiral heterocyclic β-amino esters. A new versatile access to pyrrolizidine and quinolizidine alkaloids

Ledoux, Stéphane,Marchalant, Elisabeth,Célérier, Jean-Pierre,Lhommet, Gérard

, p. 5397 - 5399 (2001)

Chiral heterocyclic β-amino esters can be easily transformed into bicyclic alkaloids after a diastereoselective alkylation followed by specific chemical transformations.

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