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38863-02-4

2-benzoyloxy-benzo[de]isoquinoline-1,3-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 38863-02-4 Structure

  • Basic information

    1. Product Name: 2-benzoyloxy-benzo[de]isoquinoline-1,3-dione
    2. Synonyms:
    3. CAS NO:38863-02-4
    4. Molecular Formula:
    5. Molecular Weight: 317.301
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 38863-02-4.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-benzoyloxy-benzo[de]isoquinoline-1,3-dione(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-benzoyloxy-benzo[de]isoquinoline-1,3-dione(38863-02-4)
    11. EPA Substance Registry System: 2-benzoyloxy-benzo[de]isoquinoline-1,3-dione(38863-02-4)

  • 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: 38863-02-4(Hazardous Substances Data)

38863-02-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38863-02-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,8,6 and 3 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 38863-02:
(7*3)+(6*8)+(5*8)+(4*6)+(3*3)+(2*0)+(1*2)=144
144 % 10 = 4
So 38863-02-4 is a valid CAS Registry Number.

38863-02-4Downstream Products

38863-02-4Relevant articles and documents

N-Aroyloxynaphthalimides as novel highly efficient DNA photocleavers: Substituent effects

Qian, Xuhong,Yao, Wei,Chen, Gang,Huang, Xiayu,Mao, Ping

, p. 6175 - 6178 (2001)

A novel DNA photocleaver family of N-benzoyloxythioxonaphthalimides, which show improved DNA intercalation and photocleaving activity compared with their oxo- counterparts, were synthesized and evaluated. The substituents on the benzene ring of the benzoyloxy moiety have an important and unusual influence on the DNA photocleaving activity. N-(p-Methoxylbenzoyloxy)thioxonaphthalimide is able to photocleave DNA at low concentration (5 μM) with 'time-resolved' and pH independent properties.

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