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104746-09-0

C14H16OP(1+)*I(1-) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 104746-09-0 Structure

  • Basic information

    1. Product Name: C14H16OP(1+)*I(1-)
    2. Synonyms:
    3. CAS NO:104746-09-0
    4. Molecular Formula:
    5. Molecular Weight: 358.159
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 104746-09-0.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: C14H16OP(1+)*I(1-)(CAS DataBase Reference)
    10. NIST Chemistry Reference: C14H16OP(1+)*I(1-)(104746-09-0)
    11. EPA Substance Registry System: C14H16OP(1+)*I(1-)(104746-09-0)

  • 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: 104746-09-0(Hazardous Substances Data)

104746-09-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 104746-09-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,7,4 and 6 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 104746-09:
(8*1)+(7*0)+(6*4)+(5*7)+(4*4)+(3*6)+(2*0)+(1*9)=110
110 % 10 = 0
So 104746-09-0 is a valid CAS Registry Number.

104746-09-0Downstream Products

104746-09-0Relevant articles and documents

Alkoxyphosphonium Salts. 4. Kinetics and Mechanisms of Arbuzov Reactions

Lewis, Edward S.,Hamp, Donald

, p. 2025 - 2029 (1983)

The kinetics of the Arbuzov reactions of trivalent phosphorus esters of the type ABPOCH3 catalyzed by CH3X have been studied.The alkoxyphosphonium ion ABCH3POCH3+ is always intermediate but often undetected.In all cases studied using methyl iodide, the rate-determining step is the alkylation of the trivalent phosphorus and the intermediate alkoxyphosphonium ion does not accumulate detectibly by NMR.In all cases with methyl triflate, the alkylation is fast and complete, and the resulting alkoxyphosphonium salt then has a constant concentration.It methylates the triv alent compound (if any remains) in a measurably slow reaction, the only observed process.This reaction represents the pure "autocatalytic" mechanism.With dimethyl sulfate the intermediate accumulates but does not ordinarily persist, and the reaction course is best fit by a combination of the "autocatalytic" mechanism with attack on the intermediate phosphonium ion by ABPOCH3 and the "textbook" mechanism in which the intermediate alkoxyphosphonium ion is dealkylated by attack of the methyl sulfate anion.

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