Welcome to LookChem.com Sign In|Join Free

CAS

  • or

58497-34-0

Post Buying Request

58497-34-0 Suppliers

Recommended suppliersmore

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

58497-34-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58497-34-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,4,9 and 7 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 58497-34:
(7*5)+(6*8)+(5*4)+(4*9)+(3*7)+(2*3)+(1*4)=170
170 % 10 = 0
So 58497-34-0 is a valid CAS Registry Number.

58497-34-0Relevant articles and documents

Isolation of functionalized phenolic monomers through selective oxidation and CO bond cleavage of the β-O-4 linkages in Lignin

Lancefield, Christopher S.,Ojo, O. Stephen,Tran, Fanny,Westwood, Nicholas J.

supporting information, p. 258 - 262 (2015/02/19)

Functionalized phenolic monomers have been generated and isolated from an organosolv lignin through a two-step depolymerization process. Chemoselective catalytic oxidation of β-O-4 linkages promoted by the DDQ/tBuONO/ O2 system was achieved in model compounds, including polymeric models and in real lignin. The oxidized β-O-4 linkages were then cleaved on reaction with zinc. Compared to many existing methods, this protocol, which can be achieved in one pot, is highly selective, giving rise to a simple mixture of products that can be readily purified to give pure compounds. The functionality present in these products makes them potentially valuable building blocks.

Electroorganic Reactions. 38. Mechanism of Electrooxidative Cleavage of Lignin Model Dimers

Pardini, Vera L.,Smith, Carmen Z.,Utley, James H. P.,Vargas, Reinaldo R.,Viertler, Hans

, p. 7305 - 7313 (2007/10/02)

The mechanisms for oxidative cleavage of several phenolic ethers, models for lignins, have been investigated by a detailed comparison of the results of anodic oxidation at nickel anodes in alkaline electrolyte with that of oxidation in acetonitrile in the presence of a triarylamine redox catalyst.The latter reaction is unambiguously initiated by single-electron transfer (SET), and in this case the major product of cleavage is aldehyde (vanillin or syringaldehyde derivatives).At nickel anodes polymerization is predominant although the aldehydes are formed together with larger amounts of the corresponding carboxylic acids.Combinations of 4-hydroxyl, α-keto, β-O-aryl, and β-hydroxymethyl functionality are shown to be crucial for the oxidation at nickel; the carboxylic acid formation probably involves a route with initial hydrogen atom abstraction at the surface.Important chemical conversions precede and accompany oxidation in alkaline media, and these are associated with the propensity for polymerization.

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 58497-34-0