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CAS

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151297-75-5

3-(4-fluorophenyl)-6-(3-pyridinyl)[1,2,4]triazolo[3,4-b][1,3,4]thiadiazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 151297-75-5 Structure

  • Basic information

    1. Product Name: 3-(4-fluorophenyl)-6-(3-pyridinyl)[1,2,4]triazolo[3,4-b][1,3,4]thiadiazole
    2. Synonyms: 3-(4-fluorophenyl)-6-(3-pyridinyl)[1,2,4]triazolo[3,4-b][1,3,4]thiadiazole
    3. CAS NO:151297-75-5
    4. Molecular Formula: C14H8FN5S
    5. Molecular Weight: 297.3102232
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 151297-75-5.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 3-(4-fluorophenyl)-6-(3-pyridinyl)[1,2,4]triazolo[3,4-b][1,3,4]thiadiazole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-(4-fluorophenyl)-6-(3-pyridinyl)[1,2,4]triazolo[3,4-b][1,3,4]thiadiazole(151297-75-5)
    11. EPA Substance Registry System: 3-(4-fluorophenyl)-6-(3-pyridinyl)[1,2,4]triazolo[3,4-b][1,3,4]thiadiazole(151297-75-5)

  • 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: 151297-75-5(Hazardous Substances Data)

151297-75-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 151297-75-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,1,2,9 and 7 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 151297-75:
(8*1)+(7*5)+(6*1)+(5*2)+(4*9)+(3*7)+(2*7)+(1*5)=135
135 % 10 = 5
So 151297-75-5 is a valid CAS Registry Number.

151297-75-5Downstream Products

151297-75-5Relevant articles and documents

Facile synthesis of 3,6-disubstituted-1,2,4-triazolo-[3,4-b]-1,3,4- thiadiazoles via oxidative cyclization of n-heteroaryl-substituted hydrazones and their biological activity

Himaja,Prathap, K. Jagadeesh,Mali, Sunil V.

, p. 823 - 828 (2012/10/29)

Fused 3,6-disubstituted triazolothiadiazoles were synthesized in good yield from a rapid and convenient oxidative cyclization of N-heteroaryl-substituted hydrazones promoted by chloramine-T trihydrate at ambient temperature. The structure of the synthesized compounds was confirmed by FTIR, 1H NMR, 13C NMR, and mass spectral data. The synthesized compounds were evaluated for their antioxidant and antitubercular activities. All the compounds 5a-i and 6a-i showed good antitubercular activity. However, only compounds 5a-i showed good antioxidant activity.

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