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CAS

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331434-05-0

4-FLUORO-N-(4H-1,2,4-TRIAZOL-4-YL)BENZENECARBOXAMIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 331434-05-0 Structure

  • Basic information

    1. Product Name: 4-FLUORO-N-(4H-1,2,4-TRIAZOL-4-YL)BENZENECARBOXAMIDE
    2. Synonyms: 4-FLUORO-N-(4H-1,2,4-TRIAZOL-4-YL)BENZENECARBOXAMIDE
    3. CAS NO:331434-05-0
    4. Molecular Formula: C9H7FN4O
    5. Molecular Weight: 206.18
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 331434-05-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.41±0.1 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
    8. Solubility: N/A
    9. PKA: 6.39±0.70(Predicted)
    10. CAS DataBase Reference: 4-FLUORO-N-(4H-1,2,4-TRIAZOL-4-YL)BENZENECARBOXAMIDE(CAS DataBase Reference)
    11. NIST Chemistry Reference: 4-FLUORO-N-(4H-1,2,4-TRIAZOL-4-YL)BENZENECARBOXAMIDE(331434-05-0)
    12. EPA Substance Registry System: 4-FLUORO-N-(4H-1,2,4-TRIAZOL-4-YL)BENZENECARBOXAMIDE(331434-05-0)

  • 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: 331434-05-0(Hazardous Substances Data)

331434-05-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 331434-05-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,1,4,3 and 4 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 331434-05:
(8*3)+(7*3)+(6*1)+(5*4)+(4*3)+(3*4)+(2*0)+(1*5)=100
100 % 10 = 0
So 331434-05-0 is a valid CAS Registry Number.

331434-05-0Downstream Products

331434-05-0Relevant articles and documents

High-yielding synthesis of N-triazolyl carboxamides via palladium-catalysed aminocarbonylation

Gergely, Máté,Boros, Borbála,Kollár, László

, p. 6736 - 6741 (2017)

Aminocarbonylation of alkenyl and aryl iodides in the presence of 4-amino-4H-1,2,4-triazole as N-nucleophile was carried out in the presence of palladium catalysts. Both types of substrates have shown high chemoselectivity toward carboxamides, i.e. practi

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