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C61H67N23O12 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1409939-01-0 Structure
  • Basic information

    1. Product Name: C61H67N23O12
    2. Synonyms:
    3. CAS NO:1409939-01-0
    4. Molecular Formula:
    5. Molecular Weight: 1314.35
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1409939-01-0.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: C61H67N23O12(CAS DataBase Reference)
    10. NIST Chemistry Reference: C61H67N23O12(1409939-01-0)
    11. EPA Substance Registry System: C61H67N23O12(1409939-01-0)
  • 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: 1409939-01-0(Hazardous Substances Data)

1409939-01-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1409939-01-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,9,9,3 and 9 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1409939-01:
(9*1)+(8*4)+(7*0)+(6*9)+(5*9)+(4*3)+(3*9)+(2*0)+(1*1)=180
180 % 10 = 0
So 1409939-01-0 is a valid CAS Registry Number.

1409939-01-0Upstream product

1409939-01-0Downstream Products

1409939-01-0Relevant articles and documents

Synthesis of cyclic Py-im polyamide libraries

Li, Benjamin C.,Montgomery, David C.,Puckett, James W.,Dervan, Peter B.

, p. 124 - 133 (2013)

Cyclic Py-Im polyamides containing two GABA turn units exhibit enhanced DNA binding affinity, but extensive studies of their biological properties have been hindered due to synthetic inaccessibility. A facile modular approach toward cyclic polyamides has been developed via microwave-assisted solid-phase synthesis of hairpin amino acid oligomer intermediates followed by macrocyclization. A focused library of cyclic polyamides 1-7 targeted to the androgen response element (ARE) and the estrogen response element (ERE) were synthesized in 12-17% overall yield. The Fmoc protection strategy also allows for selective modifications on the GABA turn units that have been shown to improve cellular uptake properties. The DNA binding affinities of a library of cyclic polyamides were measured by DNA thermal denaturation assays and compared to the corresponding hairpin polyamides. Fluorescein-labeled cyclic polyamides have been synthesized and imaged via confocal microscopy in A549 and T47D cell lines. The IC50 values of compounds 1-7 and 9-11 were determined, revealing remarkably varying levels of cytotoxicity.

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