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3-CHLORO-N-(3,5-DIMETHOXYPHENYL)-2,2-DIMETHYLPROPANAMIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 454473-71-3 Structure
  • Basic information

    1. Product Name: 3-CHLORO-N-(3,5-DIMETHOXYPHENYL)-2,2-DIMETHYLPROPANAMIDE
    2. Synonyms: 3-CHLORO-N-(3,5-DIMETHOXYPHENYL)-2,2-DIMETHYLPROPANAMIDE
    3. CAS NO:454473-71-3
    4. Molecular Formula: C13H18ClNO3
    5. Molecular Weight: 271.74
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 454473-71-3.mol
  • Chemical Properties

    1. Melting Point: 129-131°C
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 3-CHLORO-N-(3,5-DIMETHOXYPHENYL)-2,2-DIMETHYLPROPANAMIDE(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-CHLORO-N-(3,5-DIMETHOXYPHENYL)-2,2-DIMETHYLPROPANAMIDE(454473-71-3)
    11. EPA Substance Registry System: 3-CHLORO-N-(3,5-DIMETHOXYPHENYL)-2,2-DIMETHYLPROPANAMIDE(454473-71-3)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: IRRITANT
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 454473-71-3(Hazardous Substances Data)

454473-71-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 454473-71-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,5,4,4,7 and 3 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 454473-71:
(8*4)+(7*5)+(6*4)+(5*4)+(4*7)+(3*3)+(2*7)+(1*1)=163
163 % 10 = 3
So 454473-71-3 is a valid CAS Registry Number.

454473-71-3Relevant articles and documents

Copper catalyzed/mediated synthetic methodology for ebselen and related isoselenazolones

Balkrishna, Shah Jaimin,Bhakuni, Bhagat Singh,Kumar, Sangit

experimental part, p. 9565 - 9575 (2011/12/15)

Scope of the copper catalyzed/mediated selenium-nitrogen coupling reaction has been studied for the synthesis of isoselenazolones. It is noticed that the 2-chloro, 2-bromo-, and 2-iodo-aryl amides substrates can be exploited in the selenium-nitrogen coupling reaction by employing 25-100 mol % of CuI/1,10-phenanthroline (L) and potassium carbonate as a base in DMF. Furthermore, electron rich 2-chloro-arylamides also underwent selenium-nitrogen coupling reaction to give biologically important selenium-nitrogen heterocycles. Also, copper-catalyzed selenium-nitrogen coupling reaction has been meticulously applied for the synthesis of diaryl diselenides having methoxy, amine, and amide functionality from respective aryl iodides in the presence of stoichiometric amount of succinimide as an external Se-N coupling partner.

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