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220365-02-6

7-<2-(4-chlorophenyl)-2-oxoethoxy>quinolin-2(1H)-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 220365-02-6 Structure

  • Basic information

    1. Product Name: 7-<2-(4-chlorophenyl)-2-oxoethoxy>quinolin-2(1H)-one
    2. Synonyms: 7-<2-(4-chlorophenyl)-2-oxoethoxy>quinolin-2(1H)-one
    3. CAS NO:220365-02-6
    4. Molecular Formula:
    5. Molecular Weight: 313.74
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 220365-02-6.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: 7-<2-(4-chlorophenyl)-2-oxoethoxy>quinolin-2(1H)-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 7-<2-(4-chlorophenyl)-2-oxoethoxy>quinolin-2(1H)-one(220365-02-6)
    11. EPA Substance Registry System: 7-<2-(4-chlorophenyl)-2-oxoethoxy>quinolin-2(1H)-one(220365-02-6)

  • 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: 220365-02-6(Hazardous Substances Data)

220365-02-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 220365-02-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,0,3,6 and 5 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 220365-02:
(8*2)+(7*2)+(6*0)+(5*3)+(4*6)+(3*5)+(2*0)+(1*2)=86
86 % 10 = 6
So 220365-02-6 is a valid CAS Registry Number.

220365-02-6Downstream Products

220365-02-6Relevant articles and documents

Synthesis of certain quinolin-2(1H)-one α-methylene-γ-butyrolactones as potential antiplatelet agents

Chen, Yeh-Long,Wang, Tai-Chi,Fang, Kuo-Chang,Chang, Nein-Chen,Tzeng, Cherng-Chyi

, p. 453 - 462 (2007/10/03)

Certain quinolin-2(1H)-one derivatives with various α-methylene-γ- butyrolactones substituted at C(7)-position were synthesized and evaluated for their antiplatelet activity against arachidonic acid (AA)-, and platelet- activating factor (PAF)-induced aggregation in washed rabbit platelets. 7- Hydroxyquinoline 1-oxide was treated with acetic anhydride followed by the hydrolysis of 1.0 N NaOH to afford 7-hydroxyquinolin-2(1H)-one (6). The desired 7-[(2,3,4,5-tetrahydro-4-methylene-5-oxo-2-furanyl)methoxy]-quinolin- 2(1H)-ones (8a-e) were obtained from 6 via alkylation and the Reformatsky- type condensation. These quinolin-2(1H)-ones (8a-e), exhibited approximately five to seven times more potent than their coumarin counterparts against AA- and PAF-induced aggregation and are approximately two hundred times more potent than aspirin against AA-induced aggregation.

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