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82667-43-4

5-Octenyl(triphenyl)phosphoniumbromid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 82667-43-4 Structure

  • Basic information

    1. Product Name: 5-Octenyl(triphenyl)phosphoniumbromid
    2. Synonyms:
    3. CAS NO:82667-43-4
    4. Molecular Formula:
    5. Molecular Weight: 453.402
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 82667-43-4.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: 5-Octenyl(triphenyl)phosphoniumbromid(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-Octenyl(triphenyl)phosphoniumbromid(82667-43-4)
    11. EPA Substance Registry System: 5-Octenyl(triphenyl)phosphoniumbromid(82667-43-4)

  • 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: 82667-43-4(Hazardous Substances Data)

82667-43-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82667-43-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,6,6 and 7 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 82667-43:
(7*8)+(6*2)+(5*6)+(4*6)+(3*7)+(2*4)+(1*3)=154
154 % 10 = 4
So 82667-43-4 is a valid CAS Registry Number.

82667-43-4Downstream Products

82667-43-4Relevant articles and documents

Synthesis of (2E,4Z)-2,4,11-Dodecatrien-1-al, a Degradation Product of Linolenic Acid

Bohlmann, Ferdinand,Rotard, Wolfgang

, p. 1216 - 1219 (2007/10/02)

(2E,4Z)-2,4,11-Dodecatrien-1-al (13) has been prepared by using β-bromoallyl alcohol (9) and 1,8-nonadiyne (10) as starting materials. 13 is in agreement with all properties of the natural compound.The synthesis via a Wittig reaction, however, leads to a partial isomerisation of the terminal double bond.

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