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1608154-92-2

3,4,6,7,8,9-hexahydro-2-methyl-4-phenyl-2H-2-benzazepine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1608154-92-2 Structure

  • Basic information

    1. Product Name: 3,4,6,7,8,9-hexahydro-2-methyl-4-phenyl-2H-2-benzazepine
    2. Synonyms: 3,4,6,7,8,9-hexahydro-2-methyl-4-phenyl-2H-2-benzazepine
    3. CAS NO:1608154-92-2
    4. Molecular Formula:
    5. Molecular Weight: 239.36
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1608154-92-2.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: 3,4,6,7,8,9-hexahydro-2-methyl-4-phenyl-2H-2-benzazepine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3,4,6,7,8,9-hexahydro-2-methyl-4-phenyl-2H-2-benzazepine(1608154-92-2)
    11. EPA Substance Registry System: 3,4,6,7,8,9-hexahydro-2-methyl-4-phenyl-2H-2-benzazepine(1608154-92-2)

  • 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: 1608154-92-2(Hazardous Substances Data)

1608154-92-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1608154-92-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,0,8,1,5 and 4 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1608154-92:
(9*1)+(8*6)+(7*0)+(6*8)+(5*1)+(4*5)+(3*4)+(2*9)+(1*2)=162
162 % 10 = 2
So 1608154-92-2 is a valid CAS Registry Number.

1608154-92-2Downstream Products

1608154-92-2Relevant articles and documents

An investigation of the scope of the 1,7-electrocyclization of α,β:γ,δ-conjugated azomethine ylides

Zhang, Weimin,Ning, Fuqiang,Váradi, Linda,Hibbs, David E.,Platts, James A.,Nyerges, Miklós,Anderson, Rosaleen J.,Groundwater, Paul W.

, p. 3621 - 3629 (2014)

Substituents on the diene component have little influence on the periselectivity of the cyclizations of α,β:γ,δ-conjugated azomethine ylides, with 1,7-electrocyclizations predominating. In some cases, subtle changes to these substituents can, however, influence the product formed, through their effect on the relative energies of the transition states for the 1,5- (6π) and 1,7-electrocyclization (8π) processes. The most striking changes in periselectivity occur for phenylethenyl-substituted azomethine ylides 3d-f, which can give either a pyrroline 4d,f or dihydrobenzazepine 6e, depending upon the alkene configuration.

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