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1428343-07-0

C30H46N4O3SSi is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1428343-07-0 Structure

  • Basic information

    1. Product Name: C30H46N4O3SSi
    2. Synonyms: C30H46N4O3SSi
    3. CAS NO:1428343-07-0
    4. Molecular Formula:
    5. Molecular Weight: 570.872
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1428343-07-0.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: C30H46N4O3SSi(CAS DataBase Reference)
    10. NIST Chemistry Reference: C30H46N4O3SSi(1428343-07-0)
    11. EPA Substance Registry System: C30H46N4O3SSi(1428343-07-0)

  • 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: 1428343-07-0(Hazardous Substances Data)

1428343-07-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1428343-07-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,8,3,4 and 3 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1428343-07:
(9*1)+(8*4)+(7*2)+(6*8)+(5*3)+(4*4)+(3*3)+(2*0)+(1*7)=150
150 % 10 = 0
So 1428343-07-0 is a valid CAS Registry Number.

1428343-07-0Downstream Products

1428343-07-0Relevant articles and documents

The total synthesis of corallopyronin A and myxopyronin B

Rentsch, Andreas,Kalesse, Markus

, p. 11381 - 11384 (2012)

Leading the way: The synthesis of natural products with new biological targets is one of the driving forces for the development of new antibiotics. The synthesis of the two secondary metabolites corallopyronin and myxopyronin (see picture) have been achieved, which are prominent leads for the inhibition of bacterial RNA polymerase. Copyright

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