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  • 142764-36-1 Structure
  • Basic information

    1. Product Name: C21H29NO4P
    2. Synonyms:
    3. CAS NO:142764-36-1
    4. Molecular Formula:
    5. Molecular Weight: 390.439
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 142764-36-1.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: C21H29NO4P(CAS DataBase Reference)
    10. NIST Chemistry Reference: C21H29NO4P(142764-36-1)
    11. EPA Substance Registry System: C21H29NO4P(142764-36-1)
  • 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: 142764-36-1(Hazardous Substances Data)

142764-36-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 142764-36-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,2,7,6 and 4 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 142764-36:
(8*1)+(7*4)+(6*2)+(5*7)+(4*6)+(3*4)+(2*3)+(1*6)=131
131 % 10 = 1
So 142764-36-1 is a valid CAS Registry Number.

142764-36-1Downstream Products

142764-36-1Relevant articles and documents

The Mechanistic Diversity of the Thermal and Photochemical Decomposition of Bis(phenylphosphonoyl)Peroxides: Concerted Polar, Homolytic and Electron-Transfer Processes. On the Reactivity of (Phenylphosponoyl)oxyl Radicals

Korth, Hans-Gert,Lommes, Petra

, p. 2419 - 2438 (2007/10/02)

The thermal and photochemical decomposition of the first bis(phenylphosphonoyl)peroxides, dioxybis (5), and dioxybis (6) has been studied in various solvents by 1H-, 13C-, and 31P-NMR spectroscopy, laser flash photolysis (LFP), and ESR spin-trapping experiments.Kinetic studies reveal at 20 deg C a ca. 270 times slower thermal decay for 5 than for 6, which primarily results from a lower A factor rather than differences in the activation energies.The thermal decay of 5 occurs predominantly by a novel, presumably concerted polar rearrangement with formation of a thermally unstable, mixed phosphonoyl-phosphoryl anhydride.Photolysis of 5 induces homolytical cleavage of the peroxy bond with release of oxyl radicals 7.Radical 7 is characterized by a broad, transient UV/Vis absorption spectrum in the 400 to >700 nm range (λmax ca. 580 nm), as has been demonstrated by 248-nm LFP of 5 in acetonitrile solution.The short lifetime of this absorption indicates an extremely high reactivity (in hydrogen abstraction and addition) of this electrophilic radical.The thermal and photochemical decomposition of peroxide 6 leads to a virtually identical product distribution, suggesting O-O bond cleavage to be the major initial reaction under both conditions.LFP at 248 and 308 nm of a solution of 6 in acetonitrile initially produces a weak, broad absorption at ca. 500 nm and stronger bands at 280 and 400 nm.The highly transient 500-nm absorption is assigned to the oxyl radical 8, the other bands are attributed to the phosphonoyloxy-substituted benzene radical cation 8Z.The formation of this species can be explained in terms of electron transfer in the first-formed oxyl radical 8 and/or the intact peroxide 6, followed by cleavage of the peroxy bond.The decay of 8Z is accompanied by the build-up of the absorption spectrum of a 1,4-dioxy-substituted biphenyl radical cation.Key Words: Oxyl radicals / Phosphonoyl peroxides / Laser flash photolysis /ESR-Spin trapping / Electron transfer

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