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124409-86-5

diethyl [3,4-difluoro-2-(2-hydroxypropyloxy)anilinyl]methylenemalonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 124409-86-5 Structure

  • Basic information

    1. Product Name: diethyl [3,4-difluoro-2-(2-hydroxypropyloxy)anilinyl]methylenemalonate
    2. Synonyms: diethyl [3,4-difluoro-2-(2-hydroxypropyloxy)anilinyl]methylenemalonate
    3. CAS NO:124409-86-5
    4. Molecular Formula:
    5. Molecular Weight: 373.354
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 124409-86-5.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: diethyl [3,4-difluoro-2-(2-hydroxypropyloxy)anilinyl]methylenemalonate(CAS DataBase Reference)
    10. NIST Chemistry Reference: diethyl [3,4-difluoro-2-(2-hydroxypropyloxy)anilinyl]methylenemalonate(124409-86-5)
    11. EPA Substance Registry System: diethyl [3,4-difluoro-2-(2-hydroxypropyloxy)anilinyl]methylenemalonate(124409-86-5)

  • 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: 124409-86-5(Hazardous Substances Data)

124409-86-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 124409-86-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,4,0 and 9 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 124409-86:
(8*1)+(7*2)+(6*4)+(5*4)+(4*0)+(3*9)+(2*8)+(1*6)=115
115 % 10 = 5
So 124409-86-5 is a valid CAS Registry Number.

124409-86-5Relevant articles and documents

An efficient synthesis of ofloxacin and levofloxacin from 3,4- difluoroaniline

Adrio, Javier,Carretero, Juan C.,Garcia Ruano, Jose L.,Pallares, Antonio,Vicioso, Mercedes

, p. 1563 - 1572 (2007/10/03)

The functionalization at either C-2 or C-3 of N-(tert-butoxycarbonyl)- 3,4-difluoroaniline based on its ortho-deprotonation under different experimental conditions is described. This kind of products can be readily applied to the synthesis of ofloxacin, levofloxacin and related compounds.

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