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1097958-75-2

1-benzyl-3-(4-bromophenylimino)indolin-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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  • 1097958-75-2 Structure

  • Basic information

    1. Product Name: 1-benzyl-3-(4-bromophenylimino)indolin-2-one
    2. Synonyms: 1-benzyl-3-(4-bromophenylimino)indolin-2-one
    3. CAS NO:1097958-75-2
    4. Molecular Formula:
    5. Molecular Weight: 391.267
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1097958-75-2.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: 1-benzyl-3-(4-bromophenylimino)indolin-2-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-benzyl-3-(4-bromophenylimino)indolin-2-one(1097958-75-2)
    11. EPA Substance Registry System: 1-benzyl-3-(4-bromophenylimino)indolin-2-one(1097958-75-2)

  • 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: 1097958-75-2(Hazardous Substances Data)

1097958-75-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1097958-75-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,9,7,9,5 and 8 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1097958-75:
(9*1)+(8*0)+(7*9)+(6*7)+(5*9)+(4*5)+(3*8)+(2*7)+(1*5)=222
222 % 10 = 2
So 1097958-75-2 is a valid CAS Registry Number.

1097958-75-2Relevant articles and documents

α-Selective Allylation of Isatin Imines Using Metallic Barium

Yanagisawa, Akira,Yamafuji, Seiya,Sawae, Toshiki

, p. 2019 - 2023 (2016)

The Barbier-type allylation of isatin imines with allylic chlorides was achieved by using metallic barium as the promoter. Various α-allylated 3-amino-2-oxindoles were synthesized from the corresponding allylic chlorides and isatin imines. The double-bond geometry of allylic chlorides was retained throughout the reaction. An arylic bromide or iodide functionality of the products was robust to metalation under the optimum reaction conditions.

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