91214-05-0 Usage
Uses
Used in Pharmaceutical Industry:
6-OXOUNDECANOIC ACID is used as a reactant for the synthesis of various bioactive substances and pharmaceuticals for its ability to contribute to the development of new drugs and intermediates for organic synthesis.
Used in Medicinal Chemistry Research and Development:
6-OXOUNDECANOIC ACID is used as a research compound for the development of new drugs, given its potential applications in medicinal chemistry.
Used in Healthcare Industry:
6-OXOUNDECANOIC ACID is used as an antimicrobial and antifungal agent for its properties that make it useful in treating and preventing infections in various healthcare applications.
Check Digit Verification of cas no
The CAS Registry Mumber 91214-05-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,2,1 and 4 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 91214-05:
(7*9)+(6*1)+(5*2)+(4*1)+(3*4)+(2*0)+(1*5)=100
100 % 10 = 0
So 91214-05-0 is a valid CAS Registry Number.
InChI:InChI=1/C11H20O3/c1-2-3-4-7-10(12)8-5-6-9-11(13)14/h2-9H2,1H3,(H,13,14)
91214-05-0Relevant articles and documents
Indirect Electrooxidation of Alkohols and Aldehydes by Using a Double Mediatory System Consisting of RuO4/RuO2 and Cl+/Cl- Redoxes in an Aqueous-Organic Two-Phase System
Torii, Sigeru,Inokuchi, Tsutomu,Sugiura, Toyoyuki
, p. 155 - 161 (2007/10/02)
A double mediatory system consisting of RuO4/RuO2 and Cl+/Cl- redox couples has been developed for the indirect electrooxidation of alcohols and aldehydes.The reaction proceeds in the following manner: (1) oxidation of the substrate with ruthenium tetraoxide (RuO4) in the organic layer, (2) regeneration of ruthenium tetraoxide from ruthenium dioxide (RuO2) with active chlorine species (Cl2 or +), and (3) oxidation of chloride ion to + on the anode in the aqueous layer.The range of applicability of the present procedure is discussed by oxidations of (1)secondary alcohols to ketones, (2) primary alcohols and aldehydes to carboxylic acid, (3) 1,n-diols to lactones and keto acids, and (4) carbohydrate derivatives.