59020-33-6 Usage
Bicyclic structure
Two cyclopropyl rings
The compound consists of two three-membered carbon rings fused together.
Methyl groups
Attached to each cyclopropyl ring
Each of the cyclopropyl rings has a methyl group (CH3) attached to it.
Building block
Organic synthesis
It serves as a starting point for the synthesis of more complex organic compounds.
Natural occurrence
Found in various natural products
The compound can be found in some naturally occurring substances.
Potential applications
Pharmaceuticals, agrochemicals, and materials science
Due to its unique structure and reactivity, it may have uses in these industries.
Coordination chemistry
Possible use as a ligand
The compound may be utilized in coordination chemistry, potentially forming complexes with metal ions.
Catalysis
Potential use in catalysis
Further research
Required to fully understand potential applications and properties
More investigation is needed to explore the compound's full potential and characteristics.
Check Digit Verification of cas no
The CAS Registry Mumber 59020-33-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,0,2 and 0 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 59020-33:
(7*5)+(6*9)+(5*0)+(4*2)+(3*0)+(2*3)+(1*3)=106
106 % 10 = 6
So 59020-33-6 is a valid CAS Registry Number.
59020-33-6Relevant academic research and scientific papers
Dzhemilev, U. M.,Dokichev, V. A.,Sultanov, S. Z.,Khusnutdinov, R. I.,Tomilov, Yu. V.,et al.
, p. 1707 - 1714 (1989)
A systematic study has been conducted of the catalytic reaction of diazomethane with cyclic and polycyclic unsaturated hydrocarbons, conjugated dienes, as well as with a series of functionalized unsaturated conpounds.The feasibility of using transition metal, nontransition metal, and rare earth metal compounds of, for example, Co, Ni, Zr, Rh, and Dy, has been demonstrated for the first time.It has also been established that Pd(acac)2 has very high activity as a catalyst for the cyclopropanation of terminal and endocyclic double bonds by diazomethane, and that its activity is reduced upon the introduction of n-donor ligands or in the presence of strong polar solvents.
