Cas 1261298-22-9,3,3-diallyl-1-[(1S)-2-hydroxy-1-phenylethyl]piperidin-2-one

1261298-22-9

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Basic information

Product Name: 3,3-diallyl-1-[(1S)-2-hydroxy-1-phenylethyl]piperidin-2-one
Synonyms: 3,3-diallyl-1-[(1S)-2-hydroxy-1-phenylethyl]piperidin-2-one
CAS NO:1261298-22-9
Molecular Formula:
Molecular Weight: 299.413
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: 3,3-diallyl-1-[(1S)-2-hydroxy-1-phenylethyl]piperidin-2-one(CAS DataBase Reference)
NIST Chemistry Reference: 3,3-diallyl-1-[(1S)-2-hydroxy-1-phenylethyl]piperidin-2-one(1261298-22-9)
EPA Substance Registry System: 3,3-diallyl-1-[(1S)-2-hydroxy-1-phenylethyl]piperidin-2-one(1261298-22-9)

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: 1261298-22-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1261298-22-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,1,2,9 and 8 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1261298-22:
(9*1)+(8*2)+(7*6)+(6*1)+(5*2)+(4*9)+(3*8)+(2*2)+(1*2)=149
149 % 10 = 9
So 1261298-22-9 is a valid CAS Registry Number.

1261298-22-9Upstream product

1261298-17-2 C₁₉H₂₃NO₂

1261298-22-9Downstream Products

1261298-22-9Relevant academic research and scientific papers

A practical procedure for the removal of the phenylethanol moiety from phenylglycinol-derived lactams

Semak, Vladislav,Escolano, Carmen,Arroniz, Carlos,Bosch, Joan,Amat, Mercedes

experimental part, p. 2542 - 2549 (2011/02/22)

Chiral non-racemic bicyclic lactams derived from phenylglycinol have been appointed as key building blocks for the preparation of enantiopure nitrogen compounds. The removal of the chiral inductor leading to substituted piperidones by using air or oxygen

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