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CAS

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900503-43-7

ethyl 3-(8-tert-butoxycarbonyl-8-azabicyclo[3.2.1]oct-3-en-3-yl)-1H-indole-2-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 900503-43-7 Structure

  • Basic information

    1. Product Name: ethyl 3-(8-tert-butoxycarbonyl-8-azabicyclo[3.2.1]oct-3-en-3-yl)-1H-indole-2-carboxylate
    2. Synonyms:
    3. CAS NO:900503-43-7
    4. Molecular Formula: C23H28N2O4
    5. Molecular Weight: 396.4794
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 900503-43-7.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 565.685°C at 760 mmHg
    3. Flash Point: 295.916°C
    4. Appearance: N/A
    5. Density: 1.226g/cm3
    6. Vapor Pressure: 0mmHg at 25°C
    7. Refractive Index: 1.605
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: ethyl 3-(8-tert-butoxycarbonyl-8-azabicyclo[3.2.1]oct-3-en-3-yl)-1H-indole-2-carboxylate(CAS DataBase Reference)
    11. NIST Chemistry Reference: ethyl 3-(8-tert-butoxycarbonyl-8-azabicyclo[3.2.1]oct-3-en-3-yl)-1H-indole-2-carboxylate(900503-43-7)
    12. EPA Substance Registry System: ethyl 3-(8-tert-butoxycarbonyl-8-azabicyclo[3.2.1]oct-3-en-3-yl)-1H-indole-2-carboxylate(900503-43-7)

  • 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: 900503-43-7(Hazardous Substances Data)

900503-43-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 900503-43-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,0,5,0 and 3 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 900503-43:
(8*9)+(7*0)+(6*0)+(5*5)+(4*0)+(3*3)+(2*4)+(1*3)=117
117 % 10 = 7
So 900503-43-7 is a valid CAS Registry Number.

900503-43-7Downstream Products

900503-43-7Relevant articles and documents

Convenient preparation of aryl-substituted nortropanes by Suzuki-Miyaura methodology

Ghosh, Shyamali,Kinney, William A.,Gauthier, Diane A.,Lawson, Edward C.,Hudlicky, Tomas,Maryanoff, Bruce E.

, p. 555 - 560 (2007/10/03)

The synthesis of a new bicyclic vinyl boronate (5) was accomplished from N-Boc-nortropinone (6) in two steps. The Suzuki-Miyaura coupling of 5 to a variety of aryl bromides and triflates afforded 3-aryl-8-azabicyclo[3.2.1]oct-2- enes in good yields by adj

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