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763124-94-3

3-(4-methylphenyl)-4-formylsydnone thiosemicarbazone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 763124-94-3 Structure

  • Basic information

    1. Product Name: 3-(4-methylphenyl)-4-formylsydnone thiosemicarbazone
    2. Synonyms: 3-(4-methylphenyl)-4-formylsydnone thiosemicarbazone
    3. CAS NO:763124-94-3
    4. Molecular Formula:
    5. Molecular Weight: 277.307
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 763124-94-3.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-(4-methylphenyl)-4-formylsydnone thiosemicarbazone(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-(4-methylphenyl)-4-formylsydnone thiosemicarbazone(763124-94-3)
    11. EPA Substance Registry System: 3-(4-methylphenyl)-4-formylsydnone thiosemicarbazone(763124-94-3)

  • 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: 763124-94-3(Hazardous Substances Data)

763124-94-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 763124-94-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,6,3,1,2 and 4 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 763124-94:
(8*7)+(7*6)+(6*3)+(5*1)+(4*2)+(3*4)+(2*9)+(1*4)=163
163 % 10 = 3
So 763124-94-3 is a valid CAS Registry Number.

763124-94-3Downstream Products

763124-94-3Relevant articles and documents

Syntheses and evaluation of antioxidant activity of sydnonyl substituted thiazolidinone and thiazoline derivatives

Shih, Mei-Hsiu,Ke, Fang-Ying

, p. 4633 - 4643 (2004)

3-Aryl-4-formylsydnone 4′-phenylthiosemicarbazones (3a-d) and 3-aryl-4-formylsydnone thiosemicarbazones (3e-h), which are precursors of 3-aryl-4-heterocyclic sydnones, are prepared by the condensation of 3-aryl-4-formylsydnones (1a-d) with 4′-phenylthiosemicarbazide (2a) and thiosemicarbazide (2b), respectively. The thiosemicarbazones 3 reacted with cyclic reagents such as ethyl chloroacetate (4a), ethyl 2-chloroacetoacetate (4b) and 2-bromoacetophenone (4c) to produce heterocyclic substituted sydnone derivatives 5-7 that possess 4-oxo-thiazolidine and thiazoline groups. The antioxidant activity of synthesized compounds 5a-7h was evaluated. Among these compounds, 4-methyl-2-[(3-arylsydnon-4-yl-methylene)hydrazono]-2,3-dihydro- thiazole-5-carboxylic acid ethyl ester (6e-h) and 4-phenyl-2-[(3-arylsydnon-4- yl-methylene)hydrazono]-2,3-dihydro-thiazoles (7e-h) exhibit the potent DPPH (1,1-diphenyl-2-picrylhydrazyl) radical scavenging activity, comparable to that of vitamin E.

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