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CAS

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76036-40-3

3-m-Tolyl-4-aza-tricyclo[4.3.1.13,8]undecane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 76036-40-3 Structure

  • Basic information

    1. Product Name: 3-m-Tolyl-4-aza-tricyclo[4.3.1.13,8]undecane
    2. Synonyms:
    3. CAS NO:76036-40-3
    4. Molecular Formula:
    5. Molecular Weight: 241.376
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 76036-40-3.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-m-Tolyl-4-aza-tricyclo[4.3.1.13,8]undecane(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-m-Tolyl-4-aza-tricyclo[4.3.1.13,8]undecane(76036-40-3)
    11. EPA Substance Registry System: 3-m-Tolyl-4-aza-tricyclo[4.3.1.13,8]undecane(76036-40-3)

  • 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: 76036-40-3(Hazardous Substances Data)

76036-40-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76036-40-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,0,3 and 6 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 76036-40:
(7*7)+(6*6)+(5*0)+(4*3)+(3*6)+(2*4)+(1*0)=123
123 % 10 = 3
So 76036-40-3 is a valid CAS Registry Number.

76036-40-3Downstream Products

76036-40-3Relevant articles and documents

Rearrangement of 1-Azidoadamantane to 3-Aryl-4-azahomoadamantane in the Presence of Aluminum Chloride and Aromatic Substrates

Margosian, Daniel,Kovacic, Peter

, p. 877 - 880 (1981)

Reaction of 1-azidoadamantane (1) with aromatic substrates in the presence of aluminum chloride at 80 deg C for 1.25 h gave the corresponding 3-aryl-4-azahomoadamantane (2) in >90 percent yield.The reaction of 1 to 2 represents the first report of intermolecular aminoalkylation of aromatics in the benzene series, presumably from an imine intermediate.At 18 deg C, only 3-hydroxy-4-azahomoadamantane is obtained.Addition of water to the reaction system at 80 deg C yielded 1-phenyladamantane (4) as the major product.Mechanistic features are treated.

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