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154343-48-3

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

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  • 154343-48-3 Structure

  • Basic information

    1. Product Name: N-(2,5-dimethoxyphenyl)butanamide
    2. Synonyms: N-(2,5-dimethoxyphenyl)butanamide
    3. CAS NO:154343-48-3
    4. Molecular Formula: C12H17NO3
    5. Molecular Weight: 223.26828
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 154343-48-3.mol

  • Chemical Properties

    1. Melting Point: N/A
    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: N-(2,5-dimethoxyphenyl)butanamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(2,5-dimethoxyphenyl)butanamide(154343-48-3)
    11. EPA Substance Registry System: N-(2,5-dimethoxyphenyl)butanamide(154343-48-3)

  • 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: 154343-48-3(Hazardous Substances Data)

154343-48-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 154343-48-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,4,3,4 and 3 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 154343-48:
(8*1)+(7*5)+(6*4)+(5*3)+(4*4)+(3*3)+(2*4)+(1*8)=123
123 % 10 = 3
So 154343-48-3 is a valid CAS Registry Number.

154343-48-3Downstream Products

154343-48-3Relevant articles and documents

SYNTHESIS OF 2,5,8(1H)-QUINOLINETRIONE DERIVATIVES THROUGH VILSMEIER-HAACK FORMYLATION OF 2,5-DIMETHOXYANILIDES

Alonso, Miguel Angel,Blanco, M del Mar,Avendano, Carmen,Menendez, J. Carlos

, p. 2315 - 2326 (2007/10/02)

The preparation of 2,5,8(1H)-quinolinetrione derivatives bearing both electron-withdrawing and electron-releasing groups at C3 is described.The reaction sequence employed involves Vilsmeier-Haack cyclization of 2,5-dimethoxyanilides into 3-substituted 5,8-dimethoxy-2-chloroquinolinolines, followed by hydrolysis to the corresponding 2(1H)-quinolinones and oxidative demethylation with cerium ammonium nitrate.

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