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1109216-07-0

7-diethylamino-6-((4-methoxycarbonylphenyl)ethynyl)-coumarin-3-carboxylic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1109216-07-0 Structure

  • Basic information

    1. Product Name: 7-diethylamino-6-((4-methoxycarbonylphenyl)ethynyl)-coumarin-3-carboxylic acid
    2. Synonyms:
    3. CAS NO:1109216-07-0
    4. Molecular Formula:
    5. Molecular Weight: 419.434
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1109216-07-0.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-diethylamino-6-((4-methoxycarbonylphenyl)ethynyl)-coumarin-3-carboxylic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: 7-diethylamino-6-((4-methoxycarbonylphenyl)ethynyl)-coumarin-3-carboxylic acid(1109216-07-0)
    11. EPA Substance Registry System: 7-diethylamino-6-((4-methoxycarbonylphenyl)ethynyl)-coumarin-3-carboxylic acid(1109216-07-0)

  • 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: 1109216-07-0(Hazardous Substances Data)

1109216-07-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1109216-07-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,0,9,2,1 and 6 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1109216-07:
(9*1)+(8*1)+(7*0)+(6*9)+(5*2)+(4*1)+(3*6)+(2*0)+(1*7)=110
110 % 10 = 0
So 1109216-07-0 is a valid CAS Registry Number.

1109216-07-0Downstream Products

1109216-07-0Relevant articles and documents

Fluorogenic transformations based on formation of C-C bonds catalyzed by palladium: An efficient approach for high throughput optimizations and kinetic studies

Rozhkov, Roman V.,Jo Davisson,Bergstrom, Donald E.

, p. 71 - 75 (2008)

We have developed novel fluorogenic transformations based on formation of C-C bonds catalyzed by palladium using iodocoumarin 1 as a model aryl iodide, where fluorescence is quenched completely due to effects of the heavy, polarizable iodine atom. Substitution of the iodine atom for the carbon using Sonogashira, Suzuki-Miyaura and Heck couplings results in a dramatic fluorescence enhancement. This approach has been used successfully for the optimization of reaction conditions and kinetic studies in high throughput format.

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