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CAS

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1279650-21-3

3-(2-methyl-1H-indol-3-yl)-2-[mercapto(phenylamino)methylene]-3-oxopropionitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1279650-21-3 Structure

  • Basic information

    1. Product Name: 3-(2-methyl-1H-indol-3-yl)-2-[mercapto(phenylamino)methylene]-3-oxopropionitrile
    2. Synonyms:
    3. CAS NO:1279650-21-3
    4. Molecular Formula:
    5. Molecular Weight: 333.414
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1279650-21-3.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-(2-methyl-1H-indol-3-yl)-2-[mercapto(phenylamino)methylene]-3-oxopropionitrile(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-(2-methyl-1H-indol-3-yl)-2-[mercapto(phenylamino)methylene]-3-oxopropionitrile(1279650-21-3)
    11. EPA Substance Registry System: 3-(2-methyl-1H-indol-3-yl)-2-[mercapto(phenylamino)methylene]-3-oxopropionitrile(1279650-21-3)

  • 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: 1279650-21-3(Hazardous Substances Data)

1279650-21-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1279650-21-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,7,9,6,5 and 0 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1279650-21:
(9*1)+(8*2)+(7*7)+(6*9)+(5*6)+(4*5)+(3*0)+(2*2)+(1*1)=183
183 % 10 = 3
So 1279650-21-3 is a valid CAS Registry Number.

1279650-21-3Relevant articles and documents

Synthesis of new 3-substituted indole derivatives

Hassaneen, Huwaida M. E.,Pagni, Richard M.

, p. 1491 - 1497 (2010)

Treatment of 3-cyanoacetyl-2-methylindole (1) with phenyl isothiocyanate gave the corresponding thioacetanilide derivative 3. The thioacetanilide 3 was utilized as the key intermediate for the synthesis of some new 1,3,4-thiadiazole (6a, b and 9a-e), thio

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