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CAS

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1372105-03-7

2-n-butyl-6-(2-(phenylseleno)ethylamino)-1H-benzo[de]isoquinoline-1,3(2H)-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1372105-03-7 Structure

  • Basic information

    1. Product Name: 2-n-butyl-6-(2-(phenylseleno)ethylamino)-1H-benzo[de]isoquinoline-1,3(2H)-dione
    2. Synonyms:
    3. CAS NO:1372105-03-7
    4. Molecular Formula:
    5. Molecular Weight: 451.427
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1372105-03-7.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: 2-n-butyl-6-(2-(phenylseleno)ethylamino)-1H-benzo[de]isoquinoline-1,3(2H)-dione(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-n-butyl-6-(2-(phenylseleno)ethylamino)-1H-benzo[de]isoquinoline-1,3(2H)-dione(1372105-03-7)
    11. EPA Substance Registry System: 2-n-butyl-6-(2-(phenylseleno)ethylamino)-1H-benzo[de]isoquinoline-1,3(2H)-dione(1372105-03-7)

  • 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: 1372105-03-7(Hazardous Substances Data)

1372105-03-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1372105-03-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,2,1,0 and 5 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1372105-03:
(9*1)+(8*3)+(7*7)+(6*2)+(5*1)+(4*0)+(3*5)+(2*0)+(1*3)=117
117 % 10 = 7
So 1372105-03-7 is a valid CAS Registry Number.

1372105-03-7Downstream Products

1372105-03-7Relevant articles and documents

Selenium-containing naphthalimides as anticancer agents: Design, synthesis and bioactivity

Zhao, Liwei,Li, Jianfeng,Li, Yiquan,Liu, Jianwen,Wirth, Thomas,Li, Zhong

, p. 2558 - 2563 (2012)

Selenium analogues (4b-4h, and 4j) of two known sulfur compounds were synthesized and tested their anticancer activities. The selenium compound 4b had comparable activity with its sulfur analogue 4a, while DNA-binding study showed these two compounds had similar interaction with ct-DNA, the Kb was 8.23 and 2.36, respectively. The primary results showed that most compounds had moderate anticancer activities with IC50 values between 10 -6 and 10-5 M. Another selenium analogue 4j showed the highest activity with the IC50 values around 5.3 μM against K562 and MCF-7 cell lines. More importantly, the organochalcogen compounds exhibited stronger anticancer activities against K562 cell line than the other cell lines tested.

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