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111441-95-3

Phosphonium, (chloromethyl)triphenyl-, bromide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 111441-95-3 Structure

  • Basic information

    1. Product Name: Phosphonium, (chloromethyl)triphenyl-, bromide
    2. Synonyms:
    3. CAS NO:111441-95-3
    4. Molecular Formula: C19H17ClP.Br
    5. Molecular Weight: 391.675
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 111441-95-3.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: Phosphonium, (chloromethyl)triphenyl-, bromide(CAS DataBase Reference)
    10. NIST Chemistry Reference: Phosphonium, (chloromethyl)triphenyl-, bromide(111441-95-3)
    11. EPA Substance Registry System: Phosphonium, (chloromethyl)triphenyl-, bromide(111441-95-3)

  • 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: 111441-95-3(Hazardous Substances Data)

111441-95-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 111441-95-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,4,4 and 1 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 111441-95:
(8*1)+(7*1)+(6*1)+(5*4)+(4*4)+(3*1)+(2*9)+(1*5)=83
83 % 10 = 3
So 111441-95-3 is a valid CAS Registry Number.

111441-95-3Relevant articles and documents

NOVEL REACTIONS OF PHOSPHONIUM YLIDES WITH PERHALOALKANES: FIRST EXAMPLES OF HALOPHILIC ATTACKS BY PHOSPHONIUM YLIDES AND A FACILE ROUTE TO α-HALOALKYLPHOSPHONIUM SALTS

Li, Xing-Ya,Hu, Jin-Shan

, p. 6317 - 6320 (2007/10/02)

Phosphonium ylides Ph3=CHR (R = H, CH3, C2H5, n-C3H7, n-C5H11) react readily with perhalofluoroalkanes to afford regiospecifically α-haloalkylphosphonium salts Ph3P+-CHXR Y- (X = I, Br, Cl) in good yields.These reactions reveal a new type of reactivity phosphonium ylides, i.e., the halophilic attack on C-X bonds, and may be useful for the regiospecific synthesis of substituted haloolefins via Wittig reaction.

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