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122969-11-3

(3RS,1'RS)-1-methyl-3-(1'-methyl-3'-oxo-3'-phenylpropyl)2-pyrrolidinone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 122969-11-3 Structure

  • Basic information

    1. Product Name: (3RS,1'RS)-1-methyl-3-(1'-methyl-3'-oxo-3'-phenylpropyl)2-pyrrolidinone
    2. Synonyms:
    3. CAS NO:122969-11-3
    4. Molecular Formula:
    5. Molecular Weight: 245.321
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 122969-11-3.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (3RS,1'RS)-1-methyl-3-(1'-methyl-3'-oxo-3'-phenylpropyl)2-pyrrolidinone(CAS DataBase Reference)
    10. NIST Chemistry Reference: (3RS,1'RS)-1-methyl-3-(1'-methyl-3'-oxo-3'-phenylpropyl)2-pyrrolidinone(122969-11-3)
    11. EPA Substance Registry System: (3RS,1'RS)-1-methyl-3-(1'-methyl-3'-oxo-3'-phenylpropyl)2-pyrrolidinone(122969-11-3)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 122969-11-3(Hazardous Substances Data)

122969-11-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 122969-11-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,9,6 and 9 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 122969-11:
(8*1)+(7*2)+(6*2)+(5*9)+(4*6)+(3*9)+(2*1)+(1*1)=133
133 % 10 = 3
So 122969-11-3 is a valid CAS Registry Number.

122969-11-3Relevant articles and documents

Stereochemistry of the Michael Addition of N,N-Disubstituted Amide and Thioamide Enolates to α,β-Unsaturated Ketones

Oare, David A.,Henderson, Mark A.,Sanner, Mark A.,Heathcock, Clayton H.

, p. 132 - 157 (2007/10/02)

A systematic study of the regio- and diastereoselectivity of the kinetic Michael addition of amide and thioamide enolates to a series of α,β-unsaturated ketones has been carried out.Factors that influence the diastereo- and regiochemical outcome of the reaction include the substitution pattern of the enone and enolate, the enolate counterion, and the solvent.Numerous examples of high selectivity have been discovered.In a number of examples, either the syn or the anti addition products can be obtained by varying the nature of the solvent, donor atom, and/or counterion.These results have correlated in terms of a coherent transition-state model.

Stereoselection in the Michael Addition Reaction. 2. Stereochemistry of the Kinetic Michael Reaction of Amide Enolates with Enones

Heathcock, Clayton H.,Henderson, Mark A.,Oare, David A.,Sanner, Mark A.

, p. 3019 - 3022 (2007/10/02)

An extensive study of structure-stereoselectivity relationships in the kinetic Michael addition of preformed lithium enolates to enones has uncovered some reactions of sufficiently high diastereoselectivity as to be synthetically attractive and has allowe

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