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666180-03-6

4-Piperidinecarbonitrile, 4-(3,4-dimethoxyphenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 666180-03-6 Structure

  • Basic information

    1. Product Name: 4-Piperidinecarbonitrile, 4-(3,4-dimethoxyphenyl)-
    2. Synonyms:
    3. CAS NO:666180-03-6
    4. Molecular Formula: C14H18N2O2
    5. Molecular Weight: 246.309
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 666180-03-6.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: 4-Piperidinecarbonitrile, 4-(3,4-dimethoxyphenyl)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-Piperidinecarbonitrile, 4-(3,4-dimethoxyphenyl)-(666180-03-6)
    11. EPA Substance Registry System: 4-Piperidinecarbonitrile, 4-(3,4-dimethoxyphenyl)-(666180-03-6)

  • 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: 666180-03-6(Hazardous Substances Data)

666180-03-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 666180-03-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,6,6,1,8 and 0 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 666180-03:
(8*6)+(7*6)+(6*6)+(5*1)+(4*8)+(3*0)+(2*0)+(1*3)=166
166 % 10 = 6
So 666180-03-6 is a valid CAS Registry Number.

666180-03-6Relevant articles and documents

Highly potent PDE4 inhibitors with therapeutic potential

Ochiai, Hiroshi,Ohtani, Tazumi,Ishida, Akiharu,Kusumi, Kensuke,Kato, Masashi,Kohno, Hiroshi,Kishikawa, Katuya,Obata, Takaaki,Nakai, Hisao,Toda, Masaaki

, p. 207 - 210 (2007/10/03)

Based on the hypothesis that the dose-limiting side effects of PDE4 inhibitors could be mediated via the central nervous system (CNS), design and synthesis of a hydrophilic analogue is considered to be one approach to improving the side-effect profile of

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