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362485-18-5

methyl 4-[2-(trifluoromethyl)phenyl]benzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 362485-18-5 Structure

  • Basic information

    1. Product Name: methyl 4-[2-(trifluoromethyl)phenyl]benzoate
    2. Synonyms:
    3. CAS NO:362485-18-5
    4. Molecular Formula:
    5. Molecular Weight: 280.246
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 362485-18-5.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: methyl 4-[2-(trifluoromethyl)phenyl]benzoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl 4-[2-(trifluoromethyl)phenyl]benzoate(362485-18-5)
    11. EPA Substance Registry System: methyl 4-[2-(trifluoromethyl)phenyl]benzoate(362485-18-5)

  • 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: 362485-18-5(Hazardous Substances Data)

362485-18-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 362485-18-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,6,2,4,8 and 5 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 362485-18:
(8*3)+(7*6)+(6*2)+(5*4)+(4*8)+(3*5)+(2*1)+(1*8)=155
155 % 10 = 5
So 362485-18-5 is a valid CAS Registry Number.

362485-18-5Relevant articles and documents

Metal-free oxidative decarbonylative coupling of aromatic aldehydes with arenes: Direct access to biaryls

Tang, Ren-Jin,He, Qing,Yang, Luo

, p. 5925 - 5928 (2015)

A metal-free oxidative decarbonylative coupling of aromatic aldehydes with electron-rich or electron-deficient arenes to produce biaryl compounds was developed. This novel coupling was proposed to proceed via a non-chain radical homolytic aromatic substitution (HAS) type mechanism, based on the substrate scope, ortho-regioselectivity, radical trapping experiments and DFT calculation studies. With the ready availability of aromatic aldehydes and arenes, metal-free conditions should make this coupling attractive for the biaryl synthesis.

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