64836-82-4 Usage
Uses
Used in Pharmaceutical Industry:
Diethyl4-oxocyclohex-2-ene-1,1-dicarboxylate is used as a building block in organic synthesis and chemical reactions for the synthesis of various drugs. Its potential use as a ligand in coordination chemistry and its ability to undergo various chemical transformations make it a valuable component in the production of organic compounds with diverse applications in the pharmaceutical industry.
Used in Organic Synthesis:
Diethyl4-oxocyclohex-2-ene-1,1-darboxylate is used as a building block in organic synthesis for the production of various organic compounds. Its ability to undergo various chemical transformations makes it a valuable component in the synthesis of compounds with diverse applications.
Used in Coordination Chemistry:
Diethyl4-oxocyclohex-2-ene-1,1-dicarboxylate is used as a ligand in coordination chemistry, which allows for the formation of coordination compounds with various metal ions. This property makes it a valuable component in the development of new materials and catalysts.
Used in Research and Development:
Diethyl4-oxocyclohex-2-ene-1,1-dicarboxylate has demonstrated potential biological activity, which may be of interest for further research and development in pharmaceuticals and other fields. Its potential use in the synthesis of new drugs and other organic compounds makes it a valuable compound for exploration in scientific research.
Check Digit Verification of cas no
The CAS Registry Mumber 64836-82-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,8,3 and 6 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 64836-82:
(7*6)+(6*4)+(5*8)+(4*3)+(3*6)+(2*8)+(1*2)=154
154 % 10 = 4
So 64836-82-4 is a valid CAS Registry Number.
64836-82-4Relevant articles and documents
Synthesis of cobalt-substituted 1,3-diene complexes with unusual structures and their exo-selective Diels-Alder reactions
Wright, Marcus W.,Smalley Jr., Terrence L.,Welker, Mark E.,Rheingold, Arnold L.
, p. 6777 - 6791 (2007/10/02)
The synthesis and characterization (including crystallographic data) of several substituted-pyridine (Rpyr) cobalt bis(dimethylglyoxime) 1,3-butadiene complexes (R = H, tBu, 3,5-diMe, and N,N-dimethylamino) and their Diels-Alder reactions with a variety of dienophiles are reported here. The cobalt-carbon bonds in the Diels-Alder cycloadducts can be cleaved so that cobalt complexes as well as functionalized organic cycloadducts are recovered. Through these cobalt-carbon bond cleavage reactions, cobalt-diene complexes can serve as synthons for a variety of 1,3-dienes such as 1,3-butadiene, 2-(trimethylsiloxy)- 1,3-butadiene, iodoprene, (E)-1-methoxy-3-(trimethylsiloxy)-1,3-butadiene (Danishefsky's diene), and 1,2-dichloro-1,3-butadiene. The preparation of several cobalt-substituted 1,2- and 1,3-pentadiene complexes and highly exo-selective Diels-Alder reactions of the 1,3-pentadiene complexes are then discussed followed by demetalation reactions of these more highly substituted cobalt cycloadducts. These demetalation reactions maintain the stereochemical integrity found in the metal cycloadducts and also lead to cobalt recovery.
