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220938-17-0

1,11b-Dihydro-1-benzopyrano[4,3,2-de]isoquinolin-3(2H)-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 220938-17-0 Structure

  • Basic information

    1. Product Name: 1,11b-Dihydro-1-benzopyrano[4,3,2-de]isoquinolin-3(2H)-one
    2. Synonyms: GPI-6150
    3. CAS NO:220938-17-0
    4. Molecular Formula: C15H11NO2
    5. Molecular Weight: 237.26042
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 220938-17-0.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: 1,11b-Dihydro-1-benzopyrano[4,3,2-de]isoquinolin-3(2H)-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,11b-Dihydro-1-benzopyrano[4,3,2-de]isoquinolin-3(2H)-one(220938-17-0)
    11. EPA Substance Registry System: 1,11b-Dihydro-1-benzopyrano[4,3,2-de]isoquinolin-3(2H)-one(220938-17-0)

  • 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: 220938-17-0(Hazardous Substances Data)

220938-17-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 220938-17-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,0,9,3 and 8 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 220938-17:
(8*2)+(7*2)+(6*0)+(5*9)+(4*3)+(3*8)+(2*1)+(1*7)=120
120 % 10 = 0
So 220938-17-0 is a valid CAS Registry Number.

220938-17-0Downstream Products

220938-17-0Relevant articles and documents

Rh(iii)-Catalyzed intramolecular redox-neutral cyclization of alkenes via C-H activation

Shi, Zhuangzhi,Boultadakis-Arapinis, Melissa,Koester, Dennis C.,Glorius, Frank

supporting information, p. 2650 - 2652 (2014/03/21)

Biologically interesting fused oligocyclic lactams have been prepared via an intramolecular redox-neutral cyclization process. By the proper choice of the substrates with a wide variety of tethered olefins, the less favored C-H bond can be activated and f

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