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(4R,5S)-1-((E)-Hex-2-enoyl)-3,4-dimethyl-5-phenyl-imidazolidin-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 151062-79-2 Structure
  • Basic information

    1. Product Name: (4R,5S)-1-((E)-Hex-2-enoyl)-3,4-dimethyl-5-phenyl-imidazolidin-2-one
    2. Synonyms: (4R,5S)-1-((E)-Hex-2-enoyl)-3,4-dimethyl-5-phenyl-imidazolidin-2-one
    3. CAS NO:151062-79-2
    4. Molecular Formula:
    5. Molecular Weight: 286.374
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 151062-79-2.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: (4R,5S)-1-((E)-Hex-2-enoyl)-3,4-dimethyl-5-phenyl-imidazolidin-2-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: (4R,5S)-1-((E)-Hex-2-enoyl)-3,4-dimethyl-5-phenyl-imidazolidin-2-one(151062-79-2)
    11. EPA Substance Registry System: (4R,5S)-1-((E)-Hex-2-enoyl)-3,4-dimethyl-5-phenyl-imidazolidin-2-one(151062-79-2)
  • 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: 151062-79-2(Hazardous Substances Data)

151062-79-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 151062-79-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,1,0,6 and 2 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 151062-79:
(8*1)+(7*5)+(6*1)+(5*0)+(4*6)+(3*2)+(2*7)+(1*9)=102
102 % 10 = 2
So 151062-79-2 is a valid CAS Registry Number.

151062-79-2Downstream Products

151062-79-2Relevant articles and documents

Lewis Acid-Promoted 1,4-Addition to Chiral Imide Derivatives in the Synthesis of β-Amino Acids

Amoroso, Rosa,Cardillo, Giuliana,Sabatino, Piera,Tomasini, Claudia,Trere, Alessandra

, p. 5615 - 5619 (2007/10/02)

The 1,4-addition of O-benzylhydroxylamine to imides 3 in the presence of various Lewis acids is described.The reaction is performed in CH2Cl2 at -78 deg C and affords derivatives 4 and 5 in good chemical yields and in different diastereomeric ratios, depending on the Lewis acid employed.TiCl4 and Me2AlCl give opposite diastereoselectivities.Furthemore, enantiomerically pure β-amino acid 9 is obtained in good yield from compound 4a.

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