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  • 1427420-51-6 Structure
  • Basic information

    1. Product Name: C19H19NO5S
    2. Synonyms: C19H19NO5S
    3. CAS NO:1427420-51-6
    4. Molecular Formula:
    5. Molecular Weight: 373.43
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1427420-51-6.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: C19H19NO5S(CAS DataBase Reference)
    10. NIST Chemistry Reference: C19H19NO5S(1427420-51-6)
    11. EPA Substance Registry System: C19H19NO5S(1427420-51-6)
  • 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: 1427420-51-6(Hazardous Substances Data)

1427420-51-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1427420-51-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,7,4,2 and 0 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1427420-51:
(9*1)+(8*4)+(7*2)+(6*7)+(5*4)+(4*2)+(3*0)+(2*5)+(1*1)=136
136 % 10 = 6
So 1427420-51-6 is a valid CAS Registry Number.

1427420-51-6Downstream Products

1427420-51-6Relevant articles and documents

Synthesis and biological evaluation of 2-(alkoxycarbonyl)-3-anilinobenzo[b] thiophenes and thieno[2,3-b]pyridines as new potent anticancer agents

Romagnoli, Romeo,Baraldi, Pier Giovanni,Kimatrai Salvador, Maria,Preti, Delia,Aghazadeh Tabrizi, Mojgan,Bassetto, Marcella,Brancale, Andrea,Hamel, Ernest,Castagliuolo, Ignazio,Bortolozzi, Roberta,Basso, Giuseppe,Viola, Giampietro

, p. 2606 - 2618 (2013/05/09)

Two new series of inhibitors of tubulin polymerization based on the 2-(alkoxycarbonyl)-3-(3′,4′,5′-trimethoxyanilino)benzo[b] thiophene and thieno[2,3-b]pyridine molecular skeletons were synthesized and evaluated for antiproliferative activity on a panel

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