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1027077-17-3

1-[4-(4-Fluoro-phenyl)-3,6-dihydro-2H-pyridin-1-yl]-4-(1H-indol-3-yl)-butan-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1027077-17-3 Structure

  • Basic information

    1. Product Name: 1-[4-(4-Fluoro-phenyl)-3,6-dihydro-2H-pyridin-1-yl]-4-(1H-indol-3-yl)-butan-1-one
    2. Synonyms: 1-[4-(4-Fluoro-phenyl)-3,6-dihydro-2H-pyridin-1-yl]-4-(1H-indol-3-yl)-butan-1-one
    3. CAS NO:1027077-17-3
    4. Molecular Formula:
    5. Molecular Weight: 362.447
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1027077-17-3.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: 1-[4-(4-Fluoro-phenyl)-3,6-dihydro-2H-pyridin-1-yl]-4-(1H-indol-3-yl)-butan-1-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-[4-(4-Fluoro-phenyl)-3,6-dihydro-2H-pyridin-1-yl]-4-(1H-indol-3-yl)-butan-1-one(1027077-17-3)
    11. EPA Substance Registry System: 1-[4-(4-Fluoro-phenyl)-3,6-dihydro-2H-pyridin-1-yl]-4-(1H-indol-3-yl)-butan-1-one(1027077-17-3)

  • 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: 1027077-17-3(Hazardous Substances Data)

1027077-17-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1027077-17-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,7,0,7 and 7 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1027077-17:
(9*1)+(8*0)+(7*2)+(6*7)+(5*0)+(4*7)+(3*7)+(2*1)+(1*7)=123
123 % 10 = 3
So 1027077-17-3 is a valid CAS Registry Number.

1027077-17-3Relevant articles and documents

Synthesis and dopaminergic activity of some 3-(1,2,3,6-tetrahydro-1- pyridylalkyl)indoles. A novel conformational model to explain structure- activity relationships

Bottcher,Barnickel,Hausberg,Haase,Seyfried,Eiermann

, p. 4020 - 4026 (2007/10/02)

The synthesis and dopaminergic properties of a novel type of dopamine agonist is described. The number and kind of essential structural elements differ significantly from that of the rigid apomorphine-type dopamine agonists. Using standard molecular modeling techniques, a conformational model is developed proposing a U-shaped conformation which might be energetically preferred through aromatic π-π-interactions between both of the electron rich aromatic structural elements of this class of compounds. Superimposition of conformations of the lead compound 28 with apomorphine yields a novel model explaining the atypical structure-activity relationships found in this class of indolealkylamines.

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