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N-(4-chlorophenyl)-2-methoxyacetamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 104703-37-9 Structure
  • Basic information

    1. Product Name: N-(4-chlorophenyl)-2-methoxyacetamide
    2. Synonyms: N-(4-chlorophenyl)-2-methoxyacetamide
    3. CAS NO:104703-37-9
    4. Molecular Formula: C9H10ClNO2
    5. Molecular Weight: 199.6342
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 104703-37-9.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-(4-chlorophenyl)-2-methoxyacetamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(4-chlorophenyl)-2-methoxyacetamide(104703-37-9)
    11. EPA Substance Registry System: N-(4-chlorophenyl)-2-methoxyacetamide(104703-37-9)
  • 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: 104703-37-9(Hazardous Substances Data)

104703-37-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 104703-37-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,7,0 and 3 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 104703-37:
(8*1)+(7*0)+(6*4)+(5*7)+(4*0)+(3*3)+(2*3)+(1*7)=89
89 % 10 = 9
So 104703-37-9 is a valid CAS Registry Number.

104703-37-9Downstream Products

104703-37-9Relevant articles and documents

Open chair nitrogen compounds. Part X. Thermolysis of α-diazoacetanilides in methanol: a convenient synthesis of α-methoxyacetanilides from ethyl N-(arylazo)glycinate

Nicholas, Kumudini U. K. Gamage,Vaughan, Keith

, p. 799 - 802 (2007/10/02)

α-Diazoacetanilides (4), which are readily available from teh open-chair triazenes (2), undergo thermolysis in methanol solution to afford the α-methoxyacetanilides (5), an apparently rare type of ether/amide derivative.The methanolic thermolysis is inhib

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