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CAS

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303122-60-3

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

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  • 303122-60-3 Structure

  • Basic information

    1. Product Name: N-(4-acetylphenyl)-2-methoxybenzamide
    2. Synonyms: N-(4-acetylphenyl)-2-methoxybenzamide
    3. CAS NO:303122-60-3
    4. Molecular Formula: C16H15NO3
    5. Molecular Weight: 269.2952
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 303122-60-3.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-(4-acetylphenyl)-2-methoxybenzamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(4-acetylphenyl)-2-methoxybenzamide(303122-60-3)
    11. EPA Substance Registry System: N-(4-acetylphenyl)-2-methoxybenzamide(303122-60-3)

  • 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: 303122-60-3(Hazardous Substances Data)

303122-60-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 303122-60-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,3,1,2 and 2 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 303122-60:
(8*3)+(7*0)+(6*3)+(5*1)+(4*2)+(3*2)+(2*6)+(1*0)=73
73 % 10 = 3
So 303122-60-3 is a valid CAS Registry Number.

303122-60-3Downstream Products

303122-60-3Relevant articles and documents

Optimization and antifungal activity of amide analogues

Feng, Hui,Leng, Li,Liu, Jia,Tang, Yuanmou,Tang, Pengcheng,Zhang, Chixiang,Tang, Xioarong,Jiao, Shirong

, p. 4029 - 4031 (2013/05/09)

Using salicylic acid as a lead compound, a series of its analogues (compounds 1-16) were designed and synthesized. Their activity of antipathogenic fungi of plants has been evaluated in the laboratory. The results showed that these compounds had certain antifungal activity against Sclerotinia sclerotiorum and Bipolaris maydis (Nisikado et Miyake) Shoem. Among them, the inhibition of growth for 2-(3- fluorophenylcarbamoyl)phenyl acetate (1) and 2-(3-chlorophenylcarbamoyl)phenyl acetate (2) reached 91.1 %, 92.8 % and 90.1 %, 90.1 % at a concentration of 100 mg L-1, respectively.

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