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  • 20063-73-4 Structure
  • Basic information

    1. Product Name: C 684
    2. Synonyms: C 684
    3. CAS NO:20063-73-4
    4. Molecular Formula: C18H20N4O3
    5. Molecular Weight: 340.3764
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 20063-73-4.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 575.4°C at 760 mmHg
    3. Flash Point: 301.8°C
    4. Appearance: /
    5. Density: N/A
    6. Vapor Pressure: 4.43E-14mmHg at 25°C
    7. Refractive Index: N/A
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: C 684(CAS DataBase Reference)
    11. NIST Chemistry Reference: C 684(20063-73-4)
    12. EPA Substance Registry System: C 684(20063-73-4)
  • 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: 20063-73-4(Hazardous Substances Data)

20063-73-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 20063-73-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,0,6 and 3 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 20063-73:
(7*2)+(6*0)+(5*0)+(4*6)+(3*3)+(2*7)+(1*3)=64
64 % 10 = 4
So 20063-73-4 is a valid CAS Registry Number.
InChI:InChI=1/C18H21N4O3.2ClH/c1-20(2)12-6-11-19-18-13-7-3-4-8-14(13)21(23)15-9-5-10-16(17(15)18)22(24)25;;/h3-5,7-10,16,19H,6,11-12H2,1-2H3;2*1H/q-1;;

20063-73-4Upstream product

20063-73-4Downstream Products

20063-73-4Relevant articles and documents

Hypoxia-selective antitumor agents. 13. Effects of acridine substitution on the hypoxia-selective cytotoxicity and metabolic reduction of the bis- bioreductive agent nitracrine N-oxide

Lee,Wilson,Ferry,Van Zijl,Pullen,Denny

, p. 2508 - 2517 (1996)

A series of nuclear-substituted derivatives of nitracrine N-oxide (2; a bis-bioreductive hypoxia-selective cytotoxin) were prepared and evaluated, seeking analogues of lower nitroacridine reduction potential. Disubstitution with Me or OMe groups at the 4-

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