Cas 1032169-70-2,tert-butyl (2S,3S)-2-(4-fluorophenyl)-1-[(R)-1-phenylethyl]piperidine-3-carboxylate

1032169-70-2

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Basic information

Product Name: tert-butyl (2S,3S)-2-(4-fluorophenyl)-1-[(R)-1-phenylethyl]piperidine-3-carboxylate
Synonyms: tert-butyl (2S,3S)-2-(4-fluorophenyl)-1-[(R)-1-phenylethyl]piperidine-3-carboxylate
CAS NO:1032169-70-2
Molecular Formula:
Molecular Weight: 383.506
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: tert-butyl (2S,3S)-2-(4-fluorophenyl)-1-[(R)-1-phenylethyl]piperidine-3-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: tert-butyl (2S,3S)-2-(4-fluorophenyl)-1-[(R)-1-phenylethyl]piperidine-3-carboxylate(1032169-70-2)
EPA Substance Registry System: tert-butyl (2S,3S)-2-(4-fluorophenyl)-1-[(R)-1-phenylethyl]piperidine-3-carboxylate(1032169-70-2)

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: 1032169-70-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1032169-70-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,2,1,6 and 9 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1032169-70:
(9*1)+(8*0)+(7*3)+(6*2)+(5*1)+(4*6)+(3*9)+(2*7)+(1*0)=112
112 % 10 = 2
So 1032169-70-2 is a valid CAS Registry Number.

1032169-70-2Upstream product

1032169-55-3 tert-butyl (3S)-3-{allyl[(R)-1-phenylethyl]amino}-3-(4-fluorophenyl)propanoate

1032169-70-2Downstream Products

1032169-70-2Relevant academic research and scientific papers

A direct stereoselective approach to trans-2,3-disubstituted piperidines: Application in the synthesis of 2-Epi-CP-99,994 and (+)-epilupinine

Ahari, M'Hamed,Perez, Amandine,Menant, Christine,Vasse, Jean-Luc,Szymoniak, Jan

supporting information; experimental part, p. 2473 - 2476 (2009/05/27)

(Chemical Equation Presented) A simple synthesis of enantiomerically pure piperidine esters is described, offering a straightforward access to the trans-2,3-disubstituted piperidine skeleton which is present in a broad range of biologically active compounds.

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