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1407494-09-0

N,N-dimethyl-N'-(2-(4-fluorophenyl)phenyl)urea is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1407494-09-0 Structure

  • Basic information

    1. Product Name: N,N-dimethyl-N'-(2-(4-fluorophenyl)phenyl)urea
    2. Synonyms: N,N-dimethyl-N'-(2-(4-fluorophenyl)phenyl)urea
    3. CAS NO:1407494-09-0
    4. Molecular Formula:
    5. Molecular Weight: 258.295
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1407494-09-0.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: N,N-dimethyl-N'-(2-(4-fluorophenyl)phenyl)urea(CAS DataBase Reference)
    10. NIST Chemistry Reference: N,N-dimethyl-N'-(2-(4-fluorophenyl)phenyl)urea(1407494-09-0)
    11. EPA Substance Registry System: N,N-dimethyl-N'-(2-(4-fluorophenyl)phenyl)urea(1407494-09-0)

  • 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: 1407494-09-0(Hazardous Substances Data)

1407494-09-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1407494-09-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,7,4,9 and 4 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1407494-09:
(9*1)+(8*4)+(7*0)+(6*7)+(5*4)+(4*9)+(3*4)+(2*0)+(1*9)=160
160 % 10 = 0
So 1407494-09-0 is a valid CAS Registry Number.

1407494-09-0Downstream Products

1407494-09-0Relevant articles and documents

Fast and Selective Dehydrogenative C-H/C-H Arylation Using Mechanochemistry

Lou, Shao-Jie,Mao, Yang-Jie,Xu, Dan-Qian,He, Jiang-Qi,Chen, Qi,Xu, Zhen-Yuan

, p. 3890 - 3894 (2016)

A fast and site-selective biaryl synthesis via dehydrogenative C-H/C-H arylation in a ball mill was developed. In this paper, both electron-deficient oximes and electron-rich anilides quickly and under mild conditions provided arylation with various arenes to give the biaryl products in high-level selectivity. Given the solventless mechanochemical conditions, the transformation obviated the use of large amounts of arene coupling partners as solvents and allowed utilization of more-complicated and more-expensive arenes as coupling partners, which may dramatically enhance the application prospect of the C-H/C-H arylation strategy.

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