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1H-Imidazole, 1-methyl-2-phenyl-5-(trifluoromethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 63875-08-1 Structure
  • Basic information

    1. Product Name: 1H-Imidazole, 1-methyl-2-phenyl-5-(trifluoromethyl)-
    2. Synonyms:
    3. CAS NO:63875-08-1
    4. Molecular Formula: C11H9F3N2
    5. Molecular Weight: 226.201
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 63875-08-1.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: 1H-Imidazole, 1-methyl-2-phenyl-5-(trifluoromethyl)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1H-Imidazole, 1-methyl-2-phenyl-5-(trifluoromethyl)-(63875-08-1)
    11. EPA Substance Registry System: 1H-Imidazole, 1-methyl-2-phenyl-5-(trifluoromethyl)-(63875-08-1)
  • 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: 63875-08-1(Hazardous Substances Data)

63875-08-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 63875-08-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,8,7 and 5 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 63875-08:
(7*6)+(6*3)+(5*8)+(4*7)+(3*5)+(2*0)+(1*8)=151
151 % 10 = 1
So 63875-08-1 is a valid CAS Registry Number.

63875-08-1Downstream Products

63875-08-1Relevant articles and documents

4-trifluoroacetyl-2-phenyloxazol-5-one: Versatile template for syntheses of trifluoromethylsubstituted heterocycles

Saijo, Ryosuke,Kurihara, Ken-Ichi,Kawase, Masami

, p. 2533 - 2553 (2013)

4-Trifluoroacetyl-2-phenyloxazol-5-one (1) is a versatile template for the synthesis of various trifluoromethyl-substituted heterocycles. Cyclocondesation of 1 with hydroxylamine and hydrazine afforded isoxazole and pyrazole, respectively. Another key protocol involves nucleophilic ring opening of 1 with H2O or MeOH to give a-amido trifluoromethyl ketones which are transformed into trifluoromethyl-substituted thiazoles, oxazoles, imidazoles, pyrazoles, and pyrimidines.

Trifluoromethylimidazoles and a method for their preparation

-

, (2008/06/13)

4(5)-Trifluoromethylimidazoles having optional substituents in the 1 and 2 positions are provided. The novel 4(5)-trifluoromethylimidazoles are prepared by reacting a 1,1-dihalo-3,3,3-trifluoroacetone compound with an appropriate carboxaldehyde and ammoni

2-Pyrazinyl-trifluoromethylimidazoles and a method for their preparation

-

, (2008/06/13)

4(5)-Trifluoromethylimidazoles having optional substituents in the 1 and 2 positions are provided. The novel 4(5)-trifluoromethylimidazoles are prepared by reacting a 1,1-dihalo-3,3,3-trifluoroacetone compound with an appropriate carboxaldehyde and ammoni

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