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CAS

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1441224-39-0

3-(tert-butylcarbamoyl)-1-methyl-5-nitro-2-oxoindolin-3-yl benzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1441224-39-0 Structure

  • Basic information

    1. Product Name: 3-(tert-butylcarbamoyl)-1-methyl-5-nitro-2-oxoindolin-3-yl benzoate
    2. Synonyms: 3-(tert-butylcarbamoyl)-1-methyl-5-nitro-2-oxoindolin-3-yl benzoate
    3. CAS NO:1441224-39-0
    4. Molecular Formula:
    5. Molecular Weight: 411.414
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1441224-39-0.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: 3-(tert-butylcarbamoyl)-1-methyl-5-nitro-2-oxoindolin-3-yl benzoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-(tert-butylcarbamoyl)-1-methyl-5-nitro-2-oxoindolin-3-yl benzoate(1441224-39-0)
    11. EPA Substance Registry System: 3-(tert-butylcarbamoyl)-1-methyl-5-nitro-2-oxoindolin-3-yl benzoate(1441224-39-0)

  • 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: 1441224-39-0(Hazardous Substances Data)

1441224-39-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1441224-39-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,1,2,2 and 4 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1441224-39:
(9*1)+(8*4)+(7*4)+(6*1)+(5*2)+(4*2)+(3*4)+(2*3)+(1*9)=120
120 % 10 = 0
So 1441224-39-0 is a valid CAS Registry Number.

1441224-39-0Downstream Products

1441224-39-0Relevant articles and documents

OXINDOLE COMPOUNDS, SOLVENT-FREE SYNTHESIS AND USE THEREOF

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Page/Page column 13; 18, (2014/10/18)

The present invention discloses oxindole compounds and a single step, one pot reaction for the the synthesis of oxindole derivates via a solvent free Passerini reaction of isocyanides, isatins and carboxylic acids.

Engaging isatins in solvent-free, sterically congested Passerini reaction

Kaicharla, Trinadh,Yetra, Santhivardhana Reddy,Roy, Tony,Biju, Akkattu T.

supporting information, p. 1608 - 1614 (2013/09/24)

A facile, atom-economic and environmentally-benign protocol for the synthesis of biologically important oxindole derivatives in high yields has been demonstrated by employing isatins as carbonyl compound surrogates in a Passerini reaction carried out under solvent-free conditions. Moreover, electron-deficient phenols can also be used as the acid component in this reaction. In addition, the synthetic utility of the present methodology was examined by the one-pot synthesis of oxindoles with a free -OH group at the benzylic position.

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