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CAS

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131323-68-7

4-[3-(4-Oxo-4H-chromen-7-yloxy)-propyl]-1-phenyl-piperazine-2,6-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 131323-68-7 Structure

  • Basic information

    1. Product Name: 4-[3-(4-Oxo-4H-chromen-7-yloxy)-propyl]-1-phenyl-piperazine-2,6-dione
    2. Synonyms: 4-[3-(4-Oxo-4H-chromen-7-yloxy)-propyl]-1-phenyl-piperazine-2,6-dione
    3. CAS NO:131323-68-7
    4. Molecular Formula:
    5. Molecular Weight: 392.411
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 131323-68-7.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-[3-(4-Oxo-4H-chromen-7-yloxy)-propyl]-1-phenyl-piperazine-2,6-dione(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-[3-(4-Oxo-4H-chromen-7-yloxy)-propyl]-1-phenyl-piperazine-2,6-dione(131323-68-7)
    11. EPA Substance Registry System: 4-[3-(4-Oxo-4H-chromen-7-yloxy)-propyl]-1-phenyl-piperazine-2,6-dione(131323-68-7)

  • 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: 131323-68-7(Hazardous Substances Data)

131323-68-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 131323-68-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,3,2 and 3 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 131323-68:
(8*1)+(7*3)+(6*1)+(5*3)+(4*2)+(3*3)+(2*6)+(1*8)=87
87 % 10 = 7
So 131323-68-7 is a valid CAS Registry Number.

131323-68-7Downstream Products

131323-68-7Relevant articles and documents

Dopamine autoreceptor agonists as potential antipsychotics. 2. (Aminoalkoxy)-4H-1-benzopyran-4-ones

Jaen,Wise,Heffner,Pugsley,Meltzer

, p. 248 - 256 (2007/10/02)

The synthesis and pharmacological properties of a novel type of [(arylpiperazinyl)alkoxy]-4H-1-benzopyran-4-ones with dopaminergic activity are described. The nature of the arylpiperazine (AP) moiety determines the dopamine (DA) agonist/antagonist character of this series of compounds; when the aryl portion of the AP is unsubstituted the compounds appear to be DA autoreceptor agonists while substituted aryl groups seem to impart DA antagonist activity. A heterocyclic piperazine, 7-[3-[4-(2-pyridinyl)-1-piperazinyl]propoxy]-4H-1-benzopyran-4-one (31, PD 119819) has been identified as an extremely selective DA autoreceptor agonist in tests that include [3H]haloperiodol binding, inhibition of spontaneous locomotor activity, inhibition of brain DA synthesis, inhibition of brain DA neuronal firing, stereotypy assessment, and reversal of 6-hydroxydopamine (6-OHDA) induced akinesia in rats. In addition, 31 possesses good oral activity in the Sidman avoidance test in squirrel monkeys, a predictor of clinical antipsychotic efficacy. In another primate model, 31 has been found to lack the liability for extrapyramidal side effects observed with currently available antipsychotic drugs.

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