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109628-96-8

2-CYANO-3-PYRIDIN-3-YL-THIOACRYLAMIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 109628-96-8 Structure

  • Basic information

    1. Product Name: 2-CYANO-3-PYRIDIN-3-YL-THIOACRYLAMIDE
    2. Synonyms: 2-CYANO-3-PYRIDIN-3-YL-THIOACRYLAMIDE
    3. CAS NO:109628-96-8
    4. Molecular Formula: C9H7N3S
    5. Molecular Weight: 189.24
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 109628-96-8.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: 2-CYANO-3-PYRIDIN-3-YL-THIOACRYLAMIDE(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-CYANO-3-PYRIDIN-3-YL-THIOACRYLAMIDE(109628-96-8)
    11. EPA Substance Registry System: 2-CYANO-3-PYRIDIN-3-YL-THIOACRYLAMIDE(109628-96-8)

  • 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: 109628-96-8(Hazardous Substances Data)

109628-96-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 109628-96-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,6,2 and 8 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 109628-96:
(8*1)+(7*0)+(6*9)+(5*6)+(4*2)+(3*8)+(2*9)+(1*6)=148
148 % 10 = 8
So 109628-96-8 is a valid CAS Registry Number.

109628-96-8Relevant articles and documents

Synthesis, reactions, and antiviral activity of 6′-amino-2′- thioxo-1′,2′-dihydro-3,4′-bipyridine-3′, 5′-dicarbonitrile

Attaby, Fawzy A.,Elghandour,Ali,Ibrahem, Yasser M.

, p. 695 - 709 (2008/09/21)

Nicotinaldehyde 1 reacted with 2-cyanoethanethioamide 2 to give 2-cyano-3-pyridin-3-ylprop-2-enethioamide 3, which reacted with a second mole of 2to give the corresponding 6′-amino-2′-thioxo-1′,2′- dihydro-3,4′-bipyridine-3′,5′-dicarbonitrile 6. The synthetic potentiality of compound 6 was investigated via its reaction with active halogen-containing reagents, e.g., chloroacetone, 2-chloro-3-oxobutanoate, 2-chloroacetamide, chloroaceto-nitrile, and ethyl chloroacetate, to afford the corresponding thieno[2,3-b]-pyridine derivatives. Structure elucidation of all newly synthesized heterocyclic compounds was based on the data of elemental analyses, and IR, 1H NMR, as well as mass spectra. Cytotoxicity, anti-HSV1, anti-HAV, and MBB activities were evaluated for all newly synthesized heterocyclic compounds. Copyright Taylor & Francis Group, LLC.

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