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CAS

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142787-65-3

Glycine, N-phenyl-, 2-(dithiocarboxy)hydrazide, monopotassium salt is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 142787-65-3 Structure

  • Basic information

    1. Product Name: Glycine, N-phenyl-, 2-(dithiocarboxy)hydrazide, monopotassium salt
    2. Synonyms:
    3. CAS NO:142787-65-3
    4. Molecular Formula: C9H11N3OS2.K
    5. Molecular Weight: 279.428
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 142787-65-3.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: Glycine, N-phenyl-, 2-(dithiocarboxy)hydrazide, monopotassium salt(CAS DataBase Reference)
    10. NIST Chemistry Reference: Glycine, N-phenyl-, 2-(dithiocarboxy)hydrazide, monopotassium salt(142787-65-3)
    11. EPA Substance Registry System: Glycine, N-phenyl-, 2-(dithiocarboxy)hydrazide, monopotassium salt(142787-65-3)

  • 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: 142787-65-3(Hazardous Substances Data)

142787-65-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 142787-65-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,2,7,8 and 7 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 142787-65:
(8*1)+(7*4)+(6*2)+(5*7)+(4*8)+(3*7)+(2*6)+(1*5)=153
153 % 10 = 3
So 142787-65-3 is a valid CAS Registry Number.

142787-65-3Relevant articles and documents

Synthesis, spectral studies and biological activities of some N-bridged heterocycles derived from 3-arylaminomethyl-4-amino-5-mercapto-1,2,4- triazoles

Holla,Udupa

, p. 305 - 318 (2007/10/02)

Synthesis of four 3-arylaminomethyl-4-amino-5-mercapto-1,2,4-triazoles starting from substituted anilines is described. These triazoles were employed in the synthesis of some N-bridged heterocycles carrying arylaminomethyl substituents. All the newly synthesized compounds were characterized by analytical, NMR and mass spectral studies. Some of the newly synthesized compounds were screened for their antibacterial and antiviral properties.

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