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CAS

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1364083-17-9

1-[3-(2-methylthiazol-4-yl)phenyl]-1,2,3,12b-tetrahydroimidazo[1,2-f]phenanthridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1364083-17-9 Structure

  • Basic information

    1. Product Name: 1-[3-(2-methylthiazol-4-yl)phenyl]-1,2,3,12b-tetrahydroimidazo[1,2-f]phenanthridine
    2. Synonyms: 1-[3-(2-methylthiazol-4-yl)phenyl]-1,2,3,12b-tetrahydroimidazo[1,2-f]phenanthridine
    3. CAS NO:1364083-17-9
    4. Molecular Formula:
    5. Molecular Weight: 395.528
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1364083-17-9.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-[3-(2-methylthiazol-4-yl)phenyl]-1,2,3,12b-tetrahydroimidazo[1,2-f]phenanthridine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-[3-(2-methylthiazol-4-yl)phenyl]-1,2,3,12b-tetrahydroimidazo[1,2-f]phenanthridine(1364083-17-9)
    11. EPA Substance Registry System: 1-[3-(2-methylthiazol-4-yl)phenyl]-1,2,3,12b-tetrahydroimidazo[1,2-f]phenanthridine(1364083-17-9)

  • 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: 1364083-17-9(Hazardous Substances Data)

1364083-17-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1364083-17-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,4,0,8 and 3 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1364083-17:
(9*1)+(8*3)+(7*6)+(6*4)+(5*0)+(4*8)+(3*3)+(2*1)+(1*7)=149
149 % 10 = 9
So 1364083-17-9 is a valid CAS Registry Number.

1364083-17-9Relevant articles and documents

Switching between ring closed and open N-incorporated heterocycles with tuneable charges and modular reactivity based upon 5-(2-bromoethyl) phenanthridinium bromide

Eadie, Roslyn,Richmond, Craig,Moreton, Samantha,Cronin, Leroy

, p. 2026 - 2034 (2012)

5-(2-bromoethyl)phenanthridinium bromide (BEP) undergoes a 3-step-one-pot cyclisation reaction with primary amines allowing the facile synthesis of a vast library of heterocycles. A diverse range of primary aryl amines were explored as reactants to gain insight into the product isolated as a result of the steric and electronic effects of the aryl precursors. Analysis and reaction monitoring with UV-vis and NMR spectroscopy revealed that excessively electron withdrawing groups and sterically hindered amines do not allow for isolation of the common neutral tetrahydroimidazophenanthridine (TIP) structure but allow either the isolation of the charged dihydroimadazophenanthridinium (DIP) or aminoethylphenanthridinium (AEP) products.

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