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1380233-02-2

(5,5,5-trifluoro-3-methylenepentyl)benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1380233-02-2 Structure

  • Basic information

    1. Product Name: (5,5,5-trifluoro-3-methylenepentyl)benzene
    2. Synonyms: (5,5,5-trifluoro-3-methylenepentyl)benzene
    3. CAS NO:1380233-02-2
    4. Molecular Formula:
    5. Molecular Weight: 214.23
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1380233-02-2.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: (5,5,5-trifluoro-3-methylenepentyl)benzene(CAS DataBase Reference)
    10. NIST Chemistry Reference: (5,5,5-trifluoro-3-methylenepentyl)benzene(1380233-02-2)
    11. EPA Substance Registry System: (5,5,5-trifluoro-3-methylenepentyl)benzene(1380233-02-2)

  • 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: 1380233-02-2(Hazardous Substances Data)

1380233-02-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1380233-02-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,0,2,3 and 3 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1380233-02:
(9*1)+(8*3)+(7*8)+(6*0)+(5*2)+(4*3)+(3*3)+(2*0)+(1*2)=122
122 % 10 = 2
So 1380233-02-2 is a valid CAS Registry Number.

1380233-02-2Downstream Products

1380233-02-2Relevant articles and documents

Copper-catalyzed trifluoromethylation of allylsilanes

Shimizu, Ryo,Egami, Hiromichi,Hamashima, Yoshitaka,Sodeoka, Mikiko

, p. 4577 - 4580 (2012)

CF3 on Csp3: Trifluoromethylation of allylsilane derivatives was accomplished through the use of CuI and Togni's reagent (1) under mild conditions. The reaction of allylsilanes without a substituent in the 2-position gave vinylsilane derivative

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