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1421330-79-1

C11H11F3N2O is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1421330-79-1 Structure

  • Basic information

    1. Product Name: C11H11F3N2O
    2. Synonyms:
    3. CAS NO:1421330-79-1
    4. Molecular Formula:
    5. Molecular Weight: 244.216
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1421330-79-1.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: C11H11F3N2O(CAS DataBase Reference)
    10. NIST Chemistry Reference: C11H11F3N2O(1421330-79-1)
    11. EPA Substance Registry System: C11H11F3N2O(1421330-79-1)

  • 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: 1421330-79-1(Hazardous Substances Data)

1421330-79-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1421330-79-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,1,3,3 and 0 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1421330-79:
(9*1)+(8*4)+(7*2)+(6*1)+(5*3)+(4*3)+(3*0)+(2*7)+(1*9)=111
111 % 10 = 1
So 1421330-79-1 is a valid CAS Registry Number.

1421330-79-1Downstream Products

1421330-79-1Relevant articles and documents

Design and synthesis of novel 2-methyl-4,5-substitutedbenzo[f]-3,3a,4,5- tetrahydro-pyrazolo[1,5-d][1,4]oxazepin-8(7H)-one derivatives as telomerase inhibitors

Liu, Xin-Hua,Jia, Ying-Ming,Song, Bao-An,Pang, Zhi-Xiang,Yang, Song

, p. 720 - 723 (2013/03/13)

Eight novel 4,5-tetrahydropyrazolo[1,5-d][1,4]oxazepine derivatives have been synthesized and purified to be screened for anticancer activity. By a modified TRAP assay, some titled compounds were tested against telomerase, and compound 4a showed the most potent inhibitory activity with IC50 value at 0.78 ± 0.22 μM. Western blot assays showed that compounds 4a and 4b could inhibit expression of Cyclin D1, TERT, phospho-AKT and PI3K/AKT pathway.

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