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3-(2-methyl-1H-indol-3-yl)-2-(4-oxo-3-phenylthiazolidin-2-ylidene)-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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  • 1279650-22-4 Structure
  • Basic information

    1. Product Name: 3-(2-methyl-1H-indol-3-yl)-2-(4-oxo-3-phenylthiazolidin-2-ylidene)-3-oxopropionitrile
    2. Synonyms:
    3. CAS NO:1279650-22-4
    4. Molecular Formula:
    5. Molecular Weight: 373.435
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1279650-22-4.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-(4-oxo-3-phenylthiazolidin-2-ylidene)-3-oxopropionitrile(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-(2-methyl-1H-indol-3-yl)-2-(4-oxo-3-phenylthiazolidin-2-ylidene)-3-oxopropionitrile(1279650-22-4)
    11. EPA Substance Registry System: 3-(2-methyl-1H-indol-3-yl)-2-(4-oxo-3-phenylthiazolidin-2-ylidene)-3-oxopropionitrile(1279650-22-4)
  • 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: 1279650-22-4(Hazardous Substances Data)

1279650-22-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1279650-22-4 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 2 respectively.
Calculate Digit Verification of CAS Registry Number 1279650-22:
(9*1)+(8*2)+(7*7)+(6*9)+(5*6)+(4*5)+(3*0)+(2*2)+(1*2)=184
184 % 10 = 4
So 1279650-22-4 is a valid CAS Registry Number.

1279650-22-4Downstream Products

1279650-22-4Relevant articles and documents

Synthesis of new 3-substituted indole derivatives

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

, p. 1491 - 1497 (2011/02/28)

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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