820211-65-2 Usage
Explanation
The compound's full name, which includes its position of the methyl group, the presence of the oxime group, and its geometric isomerism.
Explanation
The molecular formula representing the number of carbon (C), hydrogen (H), nitrogen (N), and oxygen (O) atoms in the compound.
Explanation
The compound is derived from 1,2-cyclododecanedione by the addition of an oxime group.
Explanation
The compound has a cyclic structure with two carbonyl (C=O) groups.
Explanation
The presence of the oxime group allows the compound to form coordination compounds with metal ions, making it a potential chelating agent.
Explanation
The compound is used in the synthesis of complex organic molecules and as a ligand in metal-catalyzed reactions.
Explanation
The compound's structure and reactivity make it valuable for developing new materials with specific properties and studying the behavior of metal ions in various systems.
Explanation
The compound has a Z (cis) configuration at the double bond, which is indicated by the (1Z)prefix in its name.
Type
Oxime derivative of 1,2-cyclododecanedione
Cyclic Structure
Cyclic diketone
Oxime Group
Potential chelating agent
Applications
Organic synthesis and coordination chemistry
Utility
Building block and tool for creating new materials
Geometric Isomerism
(1Z)-
Check Digit Verification of cas no
The CAS Registry Mumber 820211-65-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,2,0,2,1 and 1 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 820211-65:
(8*8)+(7*2)+(6*0)+(5*2)+(4*1)+(3*1)+(2*6)+(1*5)=112
112 % 10 = 2
So 820211-65-2 is a valid CAS Registry Number.
820211-65-2Relevant academic research and scientific papers
Rüedi, Georg,Oberli, Matthias A.,Nagel, Matthias,Weymuth, Christophe,Hansen, Hans-Jürgen
, p. 2315 - 2318 (2004)
Treatment of α-methylene ketones with excess sodium nitrite and aqueous HCl in THF at reduced temperatures provides an effective tool for the preparation of a variety of 1,2-diketones. The diastereoselective synthesis of the corresponding (Z)-1,2-dione monoximes could be accomplished under similar conditions, but by using only one equivalent of nitrosating reagent.
