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CAS

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78867-70-6

2-Piperidinone, 1-[2-(3,4-dimethoxyphenyl)ethyl]-5-ethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 78867-70-6 Structure

  • Basic information

    1. Product Name: 2-Piperidinone, 1-[2-(3,4-dimethoxyphenyl)ethyl]-5-ethyl-
    2. Synonyms:
    3. CAS NO:78867-70-6
    4. Molecular Formula: C17H25NO3
    5. Molecular Weight: 291.39
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 78867-70-6.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: 2-Piperidinone, 1-[2-(3,4-dimethoxyphenyl)ethyl]-5-ethyl-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Piperidinone, 1-[2-(3,4-dimethoxyphenyl)ethyl]-5-ethyl-(78867-70-6)
    11. EPA Substance Registry System: 2-Piperidinone, 1-[2-(3,4-dimethoxyphenyl)ethyl]-5-ethyl-(78867-70-6)

  • 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: 78867-70-6(Hazardous Substances Data)

78867-70-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78867-70-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,8,6 and 7 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 78867-70:
(7*7)+(6*8)+(5*8)+(4*6)+(3*7)+(2*7)+(1*0)=196
196 % 10 = 6
So 78867-70-6 is a valid CAS Registry Number.

78867-70-6Relevant articles and documents

AN ALTERNATIVE ROUTE TO (+/-)-EMETINE AND (+/-)-DIHYDROCORYNANTHEINE

Takano, Seiichi,Sato, Masayuki,Ogasawara, Kunio

, p. 799 - 801 (2007/10/02)

An alternatie synthesis of (+/-)-emetine(11) and (+/-)-dihydrocorynantheine(13) has been developed in formal sense starting from methyl 3-formylhexanoate(3).

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