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1097214-22-6

C14H13N3O2S is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1097214-22-6 Structure

  • Basic information

    1. Product Name: C14H13N3O2S
    2. Synonyms:
    3. CAS NO:1097214-22-6
    4. Molecular Formula:
    5. Molecular Weight: 287.342
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1097214-22-6.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: C14H13N3O2S(CAS DataBase Reference)
    10. NIST Chemistry Reference: C14H13N3O2S(1097214-22-6)
    11. EPA Substance Registry System: C14H13N3O2S(1097214-22-6)

  • 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: 1097214-22-6(Hazardous Substances Data)

1097214-22-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1097214-22-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,9,7,2,1 and 4 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1097214-22:
(9*1)+(8*0)+(7*9)+(6*7)+(5*2)+(4*1)+(3*4)+(2*2)+(1*2)=146
146 % 10 = 6
So 1097214-22-6 is a valid CAS Registry Number.

1097214-22-6Downstream Products

1097214-22-6Relevant articles and documents

Synthesis and Ribonucleotide reductase inhibitory activity of thiosemicarbazones

Krishnan, Kesavan,Prathiba, Kumari,Jayaprakash, Venkatesan,Basu, Arijit,Mishra, Nibha,Zhou, Bingsen,Hu, Shuya,Yen, Yun

, p. 6248 - 6250 (2008)

Ribonucleotide reductase (RR) is an important therapeutic target for anticancer drugs. The structure of human RR features a 1:1 complex of two homodimeric subunits, hRRM1 and hRRM2. Prokaryotically expressed and highly purified recombinant human RR subunits, hRRM1 and hRRM2, were used for holoenzyme-based [3H]CDP reduction in vitro assay. Ten new thiosemicarbazones (7-16) were synthesized and screened for their RR inhibitory activity. Two thiosemicarbazones derived from p-hydroxy benzaldehyde (9 and 10) were found to be active but less potent than the standard, Hydroxyurea (HU). Guided by the activity of compounds 9 and 10, 11 new thiosemicarbazones (17-27) derived from p-hydroxy benzaldehyde were prepared and screened for their RR inhibitory activity. All the 11 compounds were more potent than HU.

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