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2,8-dimethyl-5-isopropenylcycloheptapyridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

111964-01-3

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  • 111964-01-3 Structure
  • Basic information

    1. Product Name: 2,8-dimethyl-5-isopropenylcycloheptapyridine
    2. Synonyms:
    3. CAS NO:111964-01-3
    4. Molecular Formula:
    5. Molecular Weight: 215.338
    6. EINECS: N/A
    7. Product Categories: N/A
  • 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: 2,8-dimethyl-5-isopropenylcycloheptapyridine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,8-dimethyl-5-isopropenylcycloheptapyridine(111964-01-3)
    11. EPA Substance Registry System: 2,8-dimethyl-5-isopropenylcycloheptapyridine(111964-01-3)
  • 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: 111964-01-3(Hazardous Substances Data)

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111964-01-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 111964-01-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,9,6 and 4 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 111964-01:
(8*1)+(7*1)+(6*1)+(5*9)+(4*6)+(3*4)+(2*0)+(1*1)=103
103 % 10 = 3
So 111964-01-3 is a valid CAS Registry Number.

111964-01-3Downstream Products

111964-01-3Relevant academic research and scientific papers

SYNTHESIS OF SESQUITERPENE ALKALOIDS, GUAIPYRIDINE, EPIGUAIPYRIDINE AND RELATED COMPOUNDS

Okatani, Teruyo,Koyama, Junko,Tagahara, Kiyoshi,Suzuta, Yukio

, p. 595 - 597 (2007/10/02)

Synthesis of sesquiterpene alkaloids, guaipyridine, epiguaipyridine and related compounds, was accomplished by application of Diels-Alder reaction of 1,2,3-triazine with enamines.

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