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CAS

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83670-87-5

5-Methyl-3-oxa-4-aza-tricyclo[5.2.1.02,6]dec-4-ene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 83670-87-5 Structure

  • Basic information

    1. Product Name: 5-Methyl-3-oxa-4-aza-tricyclo[5.2.1.02,6]dec-4-ene
    2. Synonyms: 5-Methyl-3-oxa-4-aza-tricyclo[5.2.1.02,6]dec-4-ene
    3. CAS NO:83670-87-5
    4. Molecular Formula:
    5. Molecular Weight: 151.208
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 83670-87-5.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: 5-Methyl-3-oxa-4-aza-tricyclo[5.2.1.02,6]dec-4-ene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-Methyl-3-oxa-4-aza-tricyclo[5.2.1.02,6]dec-4-ene(83670-87-5)
    11. EPA Substance Registry System: 5-Methyl-3-oxa-4-aza-tricyclo[5.2.1.02,6]dec-4-ene(83670-87-5)

  • 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: 83670-87-5(Hazardous Substances Data)

83670-87-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83670-87-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,6,7 and 0 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 83670-87:
(7*8)+(6*3)+(5*6)+(4*7)+(3*0)+(2*8)+(1*7)=155
155 % 10 = 5
So 83670-87-5 is a valid CAS Registry Number.

83670-87-5Relevant articles and documents

Pathways in the Reactions of Nitronate Ions with Sulphonyl Halides

Pigou, Paul E.,Stirling, Charles J. M.

, p. 725 - 730 (1988)

Primary and tertiary nitronate ions and sulphonyl bromides and iodides rapidly equilibrate with the nitrohalides and sulphinate ion.Products are determined by solvent and by the occurence of cross-equilibrum reactions, some of which have single-electron-transfer mechanism.The reaction of arene-sulphinate and thiolate ions with 1,2-dibromo-2-nitro-1-phenylethane gave E-β-nitrostyrene by Z-philic elimination in both cases, but the more basic thiolate ion also gave, by protophilic elimination, 2-bromo-2-nitro-1-phenylethene.

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