Cas 911051-19-9,(2R,4R)-4-hydroxy-N,1-bis[(1R)-1-phenylethyl]-2-piperidinecarboxamide

911051-19-9

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Basic information

Product Name: (2R,4R)-4-hydroxy-N,1-bis[(1R)-1-phenylethyl]-2-piperidinecarboxamide
Synonyms: (2R,4R)-4-hydroxy-N,1-bis[(1R)-1-phenylethyl]-2-piperidinecarboxamide
CAS NO:911051-19-9
Molecular Formula:
Molecular Weight: 352.477
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: (2R,4R)-4-hydroxy-N,1-bis[(1R)-1-phenylethyl]-2-piperidinecarboxamide(CAS DataBase Reference)
NIST Chemistry Reference: (2R,4R)-4-hydroxy-N,1-bis[(1R)-1-phenylethyl]-2-piperidinecarboxamide(911051-19-9)
EPA Substance Registry System: (2R,4R)-4-hydroxy-N,1-bis[(1R)-1-phenylethyl]-2-piperidinecarboxamide(911051-19-9)

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: 911051-19-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 911051-19-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,1,0,5 and 1 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 911051-19:
(8*9)+(7*1)+(6*1)+(5*0)+(4*5)+(3*1)+(2*1)+(1*9)=119
119 % 10 = 9
So 911051-19-9 is a valid CAS Registry Number.

911051-19-9Upstream product

911051-19-9Downstream Products

175671-49-5 (2R,4R)-4-hydroxy-2-piperidinecarboxylic acid

911051-19-9Relevant academic research and scientific papers

The synthesis of 4-hydroxypipecolic acids by stereoselective cycloaddition of configurationally stable nitrones

Cordero, Franca M.,Bonollo, Simona,Machetti, Fabrizio,Brandi, Alberto

, p. 3235 - 3241 (2006)

The diastereoselective synthesis of trans- and cis-4-hydroxypipecolic acids has been achieved with geometry-controlled nitrone cycloaddition chemistry. The cycloaddition of 3-butenol to enantiopure C-aminocarbonyl and C-alkoxycarbonyl nitrones having a de

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