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CAS

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1197211-04-3

8-phenyl-6-(4-(trifluoromethyl)phenyl)-8H-imidazo[2,1-c][1,4]oxazine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1197211-04-3 Structure

  • Basic information

    1. Product Name: 8-phenyl-6-(4-(trifluoromethyl)phenyl)-8H-imidazo[2,1-c][1,4]oxazine
    2. Synonyms: 8-phenyl-6-(4-(trifluoromethyl)phenyl)-8H-imidazo[2,1-c][1,4]oxazine
    3. CAS NO:1197211-04-3
    4. Molecular Formula:
    5. Molecular Weight: 342.32
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1197211-04-3.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: 8-phenyl-6-(4-(trifluoromethyl)phenyl)-8H-imidazo[2,1-c][1,4]oxazine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 8-phenyl-6-(4-(trifluoromethyl)phenyl)-8H-imidazo[2,1-c][1,4]oxazine(1197211-04-3)
    11. EPA Substance Registry System: 8-phenyl-6-(4-(trifluoromethyl)phenyl)-8H-imidazo[2,1-c][1,4]oxazine(1197211-04-3)

  • 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: 1197211-04-3(Hazardous Substances Data)

1197211-04-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1197211-04-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,7,2,1 and 1 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1197211-04:
(9*1)+(8*1)+(7*9)+(6*7)+(5*2)+(4*1)+(3*1)+(2*0)+(1*4)=143
143 % 10 = 3
So 1197211-04-3 is a valid CAS Registry Number.

1197211-04-3Downstream Products

1197211-04-3Relevant articles and documents

Efficient, regioselective access to bicyclic imidazo[1,2-x]- heterocycles via gold- and base-promoted cyclization of 1-alkynylimidazoles

Laroche, Christophe,Kerwin, Sean M.

supporting information; experimental part, p. 9229 - 9232 (2010/03/01)

(Chemical Equation Presented) Reactions of 1-alkynylimidazoles involving the formation of their 2-lithio derivatives followed by addition of aldehydes or ketones are presented. The method gives access to 1-alkynyl-2-(hydroxymethyl) imidazoles which underg

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