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3,8-Diazabicyclo[3.2.1]octane, 8-(4-aminobenzoyl)-3-(phenylmethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 401514-09-8 Structure
  • Basic information

    1. Product Name: 3,8-Diazabicyclo[3.2.1]octane, 8-(4-aminobenzoyl)-3-(phenylmethyl)-
    2. Synonyms:
    3. CAS NO:401514-09-8
    4. Molecular Formula: C20H23N3O
    5. Molecular Weight: 321.422
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 401514-09-8.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: 3,8-Diazabicyclo[3.2.1]octane, 8-(4-aminobenzoyl)-3-(phenylmethyl)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3,8-Diazabicyclo[3.2.1]octane, 8-(4-aminobenzoyl)-3-(phenylmethyl)-(401514-09-8)
    11. EPA Substance Registry System: 3,8-Diazabicyclo[3.2.1]octane, 8-(4-aminobenzoyl)-3-(phenylmethyl)-(401514-09-8)
  • 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: 401514-09-8(Hazardous Substances Data)

401514-09-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 401514-09-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,1,5,1 and 4 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 401514-09:
(8*4)+(7*0)+(6*1)+(5*5)+(4*1)+(3*4)+(2*0)+(1*9)=88
88 % 10 = 8
So 401514-09-8 is a valid CAS Registry Number.

401514-09-8Downstream Products

401514-09-8Relevant articles and documents

3,8-Diazabicyclo-[3.2.1]-octane derivatives as analogues of ambasilide, a Class III antiarrhythmic agent

Villa, Stefania,Barlocco, Daniela,Cignarella, Giorgio,Papp, Gyula Julius,Balati, Beata,Takacs, Janos,Varro, Andras,Borosy, Andras,Keseru, Katalin,Matyus, Peter

, p. 495 - 506 (2007/10/03)

Ambasilide, a representative of Class III antiarrhythmics, was reported to prolong the cardiac action potential duration in the dog, with little or no effect on Ca and Na currents. We synthesised a series of ambasilide analogues, having the 3,8-diazabicyclo-[3.2.1]-octane moiety instead of the 3,7-diazabicyclo-[3.3.1]-nonane present in ambasilide. The compounds were tested both in vitro extracellular electrophysiological assays and by the conventional microelectrode technique. Most of them lengthened the effective refractory period (ERP) with no change or slight increase on the impulse conduction time (ICT). Similarly some of the tested compounds lengthened the action potential duration (APD), a typical Class III feature, without exerting any significant effect on the maximal rate of depolarization, therefore apparently lacking Class I antiarrythmic activity.

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