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CAS

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174539-24-3

5-(Ethyl cyanoacetatothiocarbamato)-3-phenylpyrazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 174539-24-3 Structure

  • Basic information

    1. Product Name: 5-(Ethyl cyanoacetatothiocarbamato)-3-phenylpyrazole
    2. Synonyms: 5-(Ethyl cyanoacetatothiocarbamato)-3-phenylpyrazole
    3. CAS NO:174539-24-3
    4. Molecular Formula:
    5. Molecular Weight: 346.434
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 174539-24-3.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: 5-(Ethyl cyanoacetatothiocarbamato)-3-phenylpyrazole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-(Ethyl cyanoacetatothiocarbamato)-3-phenylpyrazole(174539-24-3)
    11. EPA Substance Registry System: 5-(Ethyl cyanoacetatothiocarbamato)-3-phenylpyrazole(174539-24-3)

  • 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: 174539-24-3(Hazardous Substances Data)

174539-24-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 174539-24-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,4,5,3 and 9 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 174539-24:
(8*1)+(7*7)+(6*4)+(5*5)+(4*3)+(3*9)+(2*2)+(1*4)=153
153 % 10 = 3
So 174539-24-3 is a valid CAS Registry Number.

174539-24-3Relevant articles and documents

Reaction of 3-Phenyl-5-aminopyrazole with Carbon Disulfide: A Novel Synthesis of 3-(3'-Phenylpyrazol-5'-yl)-4-phenylpyrazol-2-thione as well as of Pyrazolothiazole and Pyranothiazole Derivatives

Mohareb, R. M.,Zohdi, H. F.,Wardakhan, W. W.

, p. 1391 - 1400 (1995)

3-Phenyl-5-aminopyrazole (1) reacts with carbon disulfide, followed by in situ reaction with α-haloketones 3a-c, to afford 5, 7a, and 7b, respectively.Compounds 5 and 7 were further utilized for the formation of heterocycles and their fused derivatives. - Keywords: Aminopyrazole; Pyrazolothiazole; Pyranothiazole

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