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1,2,3,4,5,6-hexahydro-2,6-methano-3-benzazocine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 64043-31-8 Structure
  • Basic information

    1. Product Name: 1,2,3,4,5,6-hexahydro-2,6-methano-3-benzazocine
    2. Synonyms: 1,2,3,4,5,6-Hexahydro-2,6-methano-3-benzazocine; 10-Azatricyclo[7.3.1.0~2,7~]trideca-2,4,6-triene; 2,6-methano-3-benzazocine, 1,2,3,4,5,6-hexahydro-; 575-19-9; 6,7-Benzomorphan
    3. CAS NO:64043-31-8
    4. Molecular Formula: C12H15N
    5. Molecular Weight: 173.2542
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 64043-31-8.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 293°C at 760 mmHg
    3. Flash Point: 137.7°C
    4. Appearance: N/A
    5. Density: 1.04g/cm3
    6. Vapor Pressure: 0.00177mmHg at 25°C
    7. Refractive Index: 1.557
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 1,2,3,4,5,6-hexahydro-2,6-methano-3-benzazocine(CAS DataBase Reference)
    11. NIST Chemistry Reference: 1,2,3,4,5,6-hexahydro-2,6-methano-3-benzazocine(64043-31-8)
    12. EPA Substance Registry System: 1,2,3,4,5,6-hexahydro-2,6-methano-3-benzazocine(64043-31-8)
  • 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: 64043-31-8(Hazardous Substances Data)

64043-31-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 64043-31-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,0,4 and 3 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 64043-31:
(7*6)+(6*4)+(5*0)+(4*4)+(3*3)+(2*3)+(1*1)=98
98 % 10 = 8
So 64043-31-8 is a valid CAS Registry Number.

64043-31-8Downstream Products

64043-31-8Relevant articles and documents

Syntheses of the opioid substructures 1,2,3,4,5,6-hexahydro-2,6-methano-3- benzazocine and 2,3,4,5-tetrahydro-1,5-methano-1H-2-benzazepine

Coe, Jotham W.,Brooks, Paige R.,Vetelino, Michael G.,Bashore, Crystal G.,Bianco, Krista,Flick, Andrew C.

, p. 953 - 954 (2011/03/18)

Concise syntheses of 1,2,3,4,5,6-hexahydro-2,6-methano-3-benzazocine (12) and 2,3,4,5-tetrahydro-1,5-methano-1H-2-benzazepine (18) are described and involve an intramolecular Friedel-Crafts alkylation and an intramolecular Heck cyclization as their respec

1,4-Bis(arylsulfonyl)-1,2,3,4-tetrahydropyridines in synthesis. Intramolecular alkylation reactions and stereoselective synthesis of anti-2,6-disubstituted piperidines

Craig, Donald,McCague, Raymond,Potter, Gerard A.,Williams, Meredith R. V.

, p. 58 - 60 (2007/10/03)

1,4-Bis(arylsulfonyl)-1,2,3,4-tetrahydropyridines 1 having R1 containing aromatic groups undergo intramolecular electrophilic aromatic substitution reactions to give benzo-fused bicyclo[3.3.1] systems with chemoselectivities which depend on the nature of the acidic reagent used. Cationic hydrogenation of the C-5-C-6 double bond in substrates 1 substituted at C-6 provides an entry to anti-2,6-disubstituted piperidines upon desulfonylation.

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