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1357471-74-9

2-benzyl-1-(4-chlorophenyl)-2H-isoindole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1357471-74-9 Structure

  • Basic information

    1. Product Name: 2-benzyl-1-(4-chlorophenyl)-2H-isoindole
    2. Synonyms:
    3. CAS NO:1357471-74-9
    4. Molecular Formula:
    5. Molecular Weight: 317.818
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1357471-74-9.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: 2-benzyl-1-(4-chlorophenyl)-2H-isoindole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-benzyl-1-(4-chlorophenyl)-2H-isoindole(1357471-74-9)
    11. EPA Substance Registry System: 2-benzyl-1-(4-chlorophenyl)-2H-isoindole(1357471-74-9)

  • 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: 1357471-74-9(Hazardous Substances Data)

1357471-74-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1357471-74-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,7,4,7 and 1 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1357471-74:
(9*1)+(8*3)+(7*5)+(6*7)+(5*4)+(4*7)+(3*1)+(2*7)+(1*4)=179
179 % 10 = 9
So 1357471-74-9 is a valid CAS Registry Number.

1357471-74-9Downstream Products

1357471-74-9Relevant articles and documents

2-Substituted-isoindoles: A novel synthetic route and a study of the iels-Alder and Michael reactions

Voitenko, Zoia V.,Sypchenko, Volodymyr V.,Levkov, Igor V.,Potikha, Lyudmila M.,Kovtunenko, Volodymyr A.,Shishkin, Oleg V.,Shishkina, Svetlana V.

, p. 615 - 618,4 (2011)

A novel one-step procedure for the synthesis of 2-substituted-isoindoles and 1-aryl-2-substituted-isoindoles is described. The procedure is based on the reaction of 2-(bromomethyl)benzaldehyde or 2-(bromomethyl)benzophenone derivatives with primary aromatic or aliphatic amines. Reactions of 1,2-diarylisoindoles with N-phenylmaleimide were studied. Refluxing the reactants in i-PrOH in the presence of triethylamine leads to the formation of Diels-Alder endo-adducts; whilst refluxing in AcOH in the presence of AcONa affords Michael adducts. The structure of the latter was confirmed by X-ray diffraction.

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