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CAS

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865082-12-8

(Z)-1-benzyl-3-[(4-trifluoromethylphenyl)(phenyl)methylene]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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  • 865082-12-8 Structure

  • Basic information

    1. Product Name: (Z)-1-benzyl-3-[(4-trifluoromethylphenyl)(phenyl)methylene]indolin-2-one
    2. Synonyms: (Z)-1-benzyl-3-[(4-trifluoromethylphenyl)(phenyl)methylene]indolin-2-one
    3. CAS NO:865082-12-8
    4. Molecular Formula:
    5. Molecular Weight: 455.479
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 865082-12-8.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: (Z)-1-benzyl-3-[(4-trifluoromethylphenyl)(phenyl)methylene]indolin-2-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: (Z)-1-benzyl-3-[(4-trifluoromethylphenyl)(phenyl)methylene]indolin-2-one(865082-12-8)
    11. EPA Substance Registry System: (Z)-1-benzyl-3-[(4-trifluoromethylphenyl)(phenyl)methylene]indolin-2-one(865082-12-8)

  • 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: 865082-12-8(Hazardous Substances Data)

865082-12-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 865082-12-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,5,0,8 and 2 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 865082-12:
(8*8)+(7*6)+(6*5)+(5*0)+(4*8)+(3*2)+(2*1)+(1*2)=178
178 % 10 = 8
So 865082-12-8 is a valid CAS Registry Number.

865082-12-8Downstream Products

865082-12-8Relevant articles and documents

Stereoselective synthesis of 3-alkylideneoxindoles using tandem in-mediated carbometalation and Pd-catalyzed cross-coupling reaction

Yanada, Reiko,Obika, Shingo,Oyama, Munetaka,Takemoto, Yoshiji

, p. 2825 - 2828 (2004)

Efficient methods for stereoselective synthesis of various (E)-, (Z)-, and disubstituted 3-alkylideneoxindoles were investigated using tandem In-mediated carbometalation and ligandless Pd-catalyzed coupling reaction.

Stereoselective synthesis of 3-alkylideneoxindoles using tandem indium-mediated carbometallation and palladium-catalyzed cross-coupling reactions

Yanada, Reiko,Obika, Shingo,Kobayashi, Yusuke,Inokuma, Tsubasa,Oyama, Munetaka,Yanada, Kazuo,Takemoto, Yoshiji

, p. 1632 - 1642 (2007/10/03)

The first efficient methods for the stereoselective synthesis of various (E)-, (Z)-, and disubstituted 3-alkylideneoxindoles via radical cyclization reactions were investigated using tandem indium-mediated carbometallation and palladium-catalyzed cross-co

Stereoselective synthesis of 3-alkylideneoxindoles via palladium-catalyzed domino reactions

Yanada, Reiko,Obika, Shingo,Inokuma, Tsubasa,Yanada, Kazuo,Yamashita, Masayuki,Ohta, Shunsaku,Takemoto, Yoshiji

, p. 6972 - 6975 (2007/10/03)

We have developed efficient catalytic methods for the stereoselective and diversity synthesis of various (E)-, (Z)-, and disubstituted 3-alkylideneoxindoles and 3-alkylidene-benzofuran-2-ones via palladium-catalyzed Heck/Suzuki-Miyaura, Heck/Heck, and Hec

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