Cas 929282-60-0,3-Piperidinecarboxylic acid, 1-[(1S)-2-hydroxy-1-phenylethyl]-2-methyl-, methyl ester, (2R,3R)-

929282-60-0

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Basic information

Product Name: 3-Piperidinecarboxylic acid, 1-[(1S)-2-hydroxy-1-phenylethyl]-2-methyl-, methyl ester, (2R,3R)-
Synonyms:
CAS NO:929282-60-0
Molecular Formula: C16H23NO3
Molecular Weight: 277.364
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: 3-Piperidinecarboxylic acid, 1-[(1S)-2-hydroxy-1-phenylethyl]-2-methyl-, methyl ester, (2R,3R)-(CAS DataBase Reference)
NIST Chemistry Reference: 3-Piperidinecarboxylic acid, 1-[(1S)-2-hydroxy-1-phenylethyl]-2-methyl-, methyl ester, (2R,3R)-(929282-60-0)
EPA Substance Registry System: 3-Piperidinecarboxylic acid, 1-[(1S)-2-hydroxy-1-phenylethyl]-2-methyl-, methyl ester, (2R,3R)-(929282-60-0)

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: 929282-60-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 929282-60-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,9,2,8 and 2 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 929282-60:
(8*9)+(7*2)+(6*9)+(5*2)+(4*8)+(3*2)+(2*6)+(1*0)=200
200 % 10 = 0
So 929282-60-0 is a valid CAS Registry Number.

929282-60-0Upstream product

869794-46-7 (3S,8aS)-5-methyl-3-phenyl-2,3,8,8a-tetrahydro-7H-oxazolo[3,2-a]pyridine-6-carboxylic acid methyl ester

929282-60-0Downstream Products

929282-60-0Relevant academic research and scientific papers

Diastereoselective reduction of bicyclic β-enamino carbonyl piperidines - Application to the total synthesis of (-)-deoxocassine

Noel, Romain,Vanucci-Bacque, Corinne,Fargeau-Bellassoued, Marie-Claude,Lhommet, Gerard

, p. 476 - 486 (2007)

The chemo- and diastereoselective reduction of chiral piperidine β-enamino esters 4 and 6 and β-enamino ketones 5 and 7 was studied and found to afford 2,3- or 2,3,6-substituted piperidines. This approach was successfully applied to the total synthesis of

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