Welcome to LookChem.com Sign In|Join Free
  • or
1,8-bis-{3-(3,5-di-t-butyl-4-hydroxyphenyl)propionamido}octane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

66014-46-8

Post Buying Request

66014-46-8 Suppliers

Recommended suppliers

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

66014-46-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66014-46-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,0,1 and 4 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 66014-46:
(7*6)+(6*6)+(5*0)+(4*1)+(3*4)+(2*4)+(1*6)=108
108 % 10 = 8
So 66014-46-8 is a valid CAS Registry Number.

66014-46-8Downstream Products

66014-46-8Relevant academic research and scientific papers

Synthesis, antioxidant properties, and reaction kinetics of aliphatic diamine bridged hindered phenols

Li,Guo,Wang,Shi

, p. 2797 - 2803 (2016)

A series of aliphatic diamine bridged hindered phenols was synthesized. Their antioxidant activity was evaluated for assessing the role of bridging groups in trapping 1,1-diphenyl-2-picrylhydrazyl radical (DPPH?) and in 2,2'-azodi(isobutyronitrile) (AIBN) induced oxidation of styrene. The study of reaction kinetics of scavenging of the peroxyl radicals demonstrated that the scavenging ability of the DPPH free radical decreased when length of the bridging groups increased. However, the ability to protect styrene from AIBN-induced oxidation increased with increased length of the bridging groups.

Process for the production of hydroxyalkylphenyl derivatives

-

, (2008/06/13)

An improved process for the production of hydroxyalkylphenyl derivatives, especially esters and amides containing hydroxyalkylphenyl groups is disclosed, which process comprises gradually adding methyl acrylate, in the presence of an alkaline catalyst, to the alkyl substituted phenolic compound, and adding to the resultant reaction mixture a suitable alcohol or amine, optionally in the presence of a second catalyst which is different from the first catalyst. The improved process results in good yields and in a reduction of undesirable by-products while avoiding isolation of the intermediates.

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 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 66014-46-8