Cas 181872-33-3,2,2,2-Trifluoro-N-{[(S)-1-((R)-2-hydroxy-1-phenyl-ethyl)-piperidin-2-yl]-diphenyl-methyl}-acetamide

181872-33-3

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Basic information

Product Name: 2,2,2-Trifluoro-N-{[(S)-1-((R)-2-hydroxy-1-phenyl-ethyl)-piperidin-2-yl]-diphenyl-methyl}-acetamide
Synonyms: 2,2,2-Trifluoro-N-{[(S)-1-((R)-2-hydroxy-1-phenyl-ethyl)-piperidin-2-yl]-diphenyl-methyl}-acetamide
CAS NO:181872-33-3
Molecular Formula:
Molecular Weight: 482.546
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: 2,2,2-Trifluoro-N-{[(S)-1-((R)-2-hydroxy-1-phenyl-ethyl)-piperidin-2-yl]-diphenyl-methyl}-acetamide(CAS DataBase Reference)
NIST Chemistry Reference: 2,2,2-Trifluoro-N-{[(S)-1-((R)-2-hydroxy-1-phenyl-ethyl)-piperidin-2-yl]-diphenyl-methyl}-acetamide(181872-33-3)
EPA Substance Registry System: 2,2,2-Trifluoro-N-{[(S)-1-((R)-2-hydroxy-1-phenyl-ethyl)-piperidin-2-yl]-diphenyl-methyl}-acetamide(181872-33-3)

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: 181872-33-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 181872-33-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,1,8,7 and 2 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 181872-33:
(8*1)+(7*8)+(6*1)+(5*8)+(4*7)+(3*2)+(2*3)+(1*3)=153
153 % 10 = 3
So 181872-33-3 is a valid CAS Registry Number.

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181872-33-3Relevant academic research and scientific papers

Asymmetric synthesis. 39. Synthesis of 2-(1-aminoalkyl)piperidines via 2-cyano-6-phenyl oxazolopiperidine

Froelich, Olivier,Desos, Patrice,Bonin, Martine,Quirion, Jean-Charles,Husson, Henri-Philippe,Zhu, Jieping

, p. 6700 - 6705 (2007/10/03)

The asymmetric synthesis of a series of 2-(1-aminoalkyl) piperidines using (-)-2-cyano-6-phenyloxazolopiperidine 1 is described. LiAlH4 reduction of 1 followed by hydrogenolysis led to the diamine 3. The same strategy applied to C-2-methylated

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