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C19H19BrN4S2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 340008-01-7 Structure
  • Basic information

    1. Product Name: C19H19BrN4S2
    2. Synonyms:
    3. CAS NO:340008-01-7
    4. Molecular Formula:
    5. Molecular Weight: 447.423
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 340008-01-7.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: C19H19BrN4S2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C19H19BrN4S2(340008-01-7)
    11. EPA Substance Registry System: C19H19BrN4S2(340008-01-7)
  • 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: 340008-01-7(Hazardous Substances Data)

340008-01-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 340008-01-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,0,0,0 and 8 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 340008-01:
(8*3)+(7*4)+(6*0)+(5*0)+(4*0)+(3*8)+(2*0)+(1*1)=77
77 % 10 = 7
So 340008-01-7 is a valid CAS Registry Number.

340008-01-7Downstream Products

340008-01-7Relevant articles and documents

Synthesis of new 4-thiazolidinones bearing potentially active heteryl moities

Ingle,Sawale,Ingle,Mane

, p. 124 - 128 (2007/10/03)

2-Acyl-3-methyl-7-substituted-1,4-benzothiazines 1A and 5-acyl-1-aryl-2-mercapto-4-methylimidazoles 1B have been converted to their respective hydrazones 2A and 2B by refluxing them with hydrazine hydrate in digol. The hydrazino derivatives on condensation with aryl isothiocyanates give asymmetric thioureas 3A and 3B. The thioureas when refluxed with monochloroacetic acid in glacial acetic acid using anhydrous sodium acetate as catalyst yield the title products, 2-[(-3′-methyl-4H-7′-substituted-1,4-benzothiazin-2′-yl) -methyl-ketoiminyl]imino-3-aryl-4-thiazolidinones 4A and 2-[(l′-substituted phenyl-2′-mercapto-4′-methylimidazol-5′-yl) -methyl-ketoiminyl]imino-3-substituted phenyl-4-thiazolidinones 4B. Some of the newly synthesised compounds have been screened against Alternaria brassicae, Gloeosporium ampelophagum and Fusarium oxysporium and the results are presented.

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