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CAS

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705972-11-8

N1-[2-(4-chlorophenyl)-2-oxoethyl]-N1-(4-methoxyphenyl)-2-phenylacetamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 705972-11-8 Structure

  • Basic information

    1. Product Name: N1-[2-(4-chlorophenyl)-2-oxoethyl]-N1-(4-methoxyphenyl)-2-phenylacetamide
    2. Synonyms: N1-[2-(4-chlorophenyl)-2-oxoethyl]-N1-(4-methoxyphenyl)-2-phenylacetamide
    3. CAS NO:705972-11-8
    4. Molecular Formula:
    5. Molecular Weight: 393.87
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 705972-11-8.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: N1-[2-(4-chlorophenyl)-2-oxoethyl]-N1-(4-methoxyphenyl)-2-phenylacetamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N1-[2-(4-chlorophenyl)-2-oxoethyl]-N1-(4-methoxyphenyl)-2-phenylacetamide(705972-11-8)
    11. EPA Substance Registry System: N1-[2-(4-chlorophenyl)-2-oxoethyl]-N1-(4-methoxyphenyl)-2-phenylacetamide(705972-11-8)

  • 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: 705972-11-8(Hazardous Substances Data)

705972-11-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 705972-11-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,0,5,9,7 and 2 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 705972-11:
(8*7)+(7*0)+(6*5)+(5*9)+(4*7)+(3*2)+(2*1)+(1*1)=168
168 % 10 = 8
So 705972-11-8 is a valid CAS Registry Number.

705972-11-8Downstream Products

705972-11-8Relevant articles and documents

Sequential One-Pot Synthesis of Imidazoles and 2H-Imidazolones from β-Ketoamines, Acylating Agents and Ammonium Acetate

Jalani, Hitesh B.,Venkateswararao, Eeda,Manickam, Manoj,Jung, Sang-Hun

supporting information, p. 1966 - 1970 (2016/12/16)

An efficient, practical, straight forward, and transition metal-free three-component synthesis of diversely substituted imidazoles and 2H-imidazolones from β-ketoamines, acylating agents, and ammonium acetate has been described herein. This approach invol

A rapid and direct access to symmetrical/unsymmetrical 3,4-diarylmaleimides and pyrrolin-2-ones

Pal, Manojit,Swamy, Nalivela Kumara,Hameed, P. Shahul,Padakanti, Srinivas,Yeleswarapu, Koteswar Rao

, p. 3987 - 3997 (2007/10/03)

1,8-Diazabicyclo[5.4.0]undec-7ene (DBU) facilitated the oxidative cyclization of phenacyl amide in the presence of atmospheric oxygen under environmentally friendly conditions. The reaction has been studied under various conditions and a plausible mechani

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