Welcome to LookChem.com Sign In|Join Free

CAS

  • or

46438-39-5

Post Buying Request

46438-39-5 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

46438-39-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 46438-39-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,6,4,3 and 8 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 46438-39:
(7*4)+(6*6)+(5*4)+(4*3)+(3*8)+(2*3)+(1*9)=135
135 % 10 = 5
So 46438-39-5 is a valid CAS Registry Number.

46438-39-5Relevant 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

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 46438-39-5