91214-05-0 Usage
General Description
6-OXOUNDECANOIC ACID, also known as 6-oxo-undecanoic acid or 6-oxoundecanoate, is a chemical compound belonging to the class of organic compounds known as medium-chain 3-keto acids and derivatives. It is a white powder with a molecular formula of C11H20O3 and a molecular weight of 200.28 g/mol. 6-OXOUNDECANOIC ACID is commonly used as a reactant for the synthesis of various bioactive substances, pharmaceuticals, and intermediates for organic synthesis. It is also used in the research and development of new drugs and has potential applications in the field of medicinal chemistry. Additionally, 6-OXOUNDECANOIC ACID is known to exhibit antimicrobial and antifungal properties, making it useful for a variety of purposes in the pharmaceutical and healthcare industries.
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.
