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CAS

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1618086-06-8

C17H17F3 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1618086-06-8 Structure

  • Basic information

    1. Product Name: C17H17F3
    2. Synonyms: C17H17F3
    3. CAS NO:1618086-06-8
    4. Molecular Formula:
    5. Molecular Weight: 278.317
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1618086-06-8.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: C17H17F3(CAS DataBase Reference)
    10. NIST Chemistry Reference: C17H17F3(1618086-06-8)
    11. EPA Substance Registry System: C17H17F3(1618086-06-8)

  • 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: 1618086-06-8(Hazardous Substances Data)

1618086-06-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1618086-06-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,1,8,0,8 and 6 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1618086-06:
(9*1)+(8*6)+(7*1)+(6*8)+(5*0)+(4*8)+(3*6)+(2*0)+(1*6)=168
168 % 10 = 8
So 1618086-06-8 is a valid CAS Registry Number.

1618086-06-8Downstream Products

1618086-06-8Relevant articles and documents

Copper-catalyzed intermolecular trifluoromethylarylation of alkenes: Mutual activation of arylboronic acid and CF3+ reagent

Wang, Fei,Wang, Dinghai,Mu, Xin,Chen, Pinhong,Liu, Guosheng

supporting information, p. 10202 - 10205 (2014/08/05)

A novel copper-catalyzed intermolecular trifluoromethylarylation of alkenes is developed using less active ether-type Togni's reagent under mild reaction conditions. Various alkenes and diverse arylboronic acids are compatible with these conditions. Preliminary mechanistic studies reveal that a mutual activation process between arylboronic acid and CF3+ reagent is essential. In addition, the reaction might involve a rate-determining transmetalation, and the final aryl C-C bond is derived from reductive elimination of the aryl(alkyl)Cu(III) intermediate.

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