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356067-04-4

3-(4-trifluoromethyl)phenylprop-2-yn-1-(4-tert-butylphenyl) ether is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 356067-04-4 Structure

  • Basic information

    1. Product Name: 3-(4-trifluoromethyl)phenylprop-2-yn-1-(4-tert-butylphenyl) ether
    2. Synonyms:
    3. CAS NO:356067-04-4
    4. Molecular Formula:
    5. Molecular Weight: 332.365
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 356067-04-4.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: 3-(4-trifluoromethyl)phenylprop-2-yn-1-(4-tert-butylphenyl) ether(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-(4-trifluoromethyl)phenylprop-2-yn-1-(4-tert-butylphenyl) ether(356067-04-4)
    11. EPA Substance Registry System: 3-(4-trifluoromethyl)phenylprop-2-yn-1-(4-tert-butylphenyl) ether(356067-04-4)

  • 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: 356067-04-4(Hazardous Substances Data)

356067-04-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 356067-04-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,6,0,6 and 7 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 356067-04:
(8*3)+(7*5)+(6*6)+(5*0)+(4*6)+(3*7)+(2*0)+(1*4)=144
144 % 10 = 4
So 356067-04-4 is a valid CAS Registry Number.

356067-04-4Downstream Products

356067-04-4Relevant articles and documents

Recognition-mediated regiocontrol of a dipolar cycloaddition reaction

Howell, Sarah J,Spencer, Neil,Philp, Douglas

, p. 4945 - 4954 (2001)

The rational design of a recognition-based system that is capable of accelerating and controlling the regiochemical outcome of a dipolar cycloaddition reaction between an azide and an alkyne is presented. The origins of the acceleration and control of the cycloaddition reactions are rationalized - using molecular mechanics calculations - in terms of the formation of a complex between the reagents which organizes and orients them prior to reaction.

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