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1304771-73-0

2-(2-methylquinoxalin-3-ylthio)-N-(2,3-dimethylphenyl)acetamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1304771-73-0 Structure

  • Basic information

    1. Product Name: 2-(2-methylquinoxalin-3-ylthio)-N-(2,3-dimethylphenyl)acetamide
    2. Synonyms:
    3. CAS NO:1304771-73-0
    4. Molecular Formula:
    5. Molecular Weight: 337.445
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1304771-73-0.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: 2-(2-methylquinoxalin-3-ylthio)-N-(2,3-dimethylphenyl)acetamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(2-methylquinoxalin-3-ylthio)-N-(2,3-dimethylphenyl)acetamide(1304771-73-0)
    11. EPA Substance Registry System: 2-(2-methylquinoxalin-3-ylthio)-N-(2,3-dimethylphenyl)acetamide(1304771-73-0)

  • 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: 1304771-73-0(Hazardous Substances Data)

1304771-73-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1304771-73-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,0,4,7,7 and 1 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1304771-73:
(9*1)+(8*3)+(7*0)+(6*4)+(5*7)+(4*7)+(3*1)+(2*7)+(1*3)=140
140 % 10 = 0
So 1304771-73-0 is a valid CAS Registry Number.

1304771-73-0Downstream Products

1304771-73-0Relevant articles and documents

Synthesis and antimicrobial activity of some new thioether derivatives of quinoxaline

Singh,Hashim,Singhal

, p. 635 - 642 (2011)

2-Chloro-3-methylquinoxaline was selected as nucleus around which the molecular manipulations were carried out to get new compounds expected to possess better anti microbial activity. Various quinoxaline derivatives have been synthesized by replacing the chlorine at C-2 with a thioether linkage, which in turn attached to 2-(N-(substituted phenyl)acetamides. The synthesized compounds (5) were tested for their antimicrobial activity. Compounds 5b, 5c, 5d and 5i were found most active (comparable to the standard antibacterial Ciprofloxacin) amongst them. The structure of the compounds was confirmed on the basis of their spectral data.

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