5467-28-7 Usage
Chemical structure
A complex structure with four carboxylate groups attached to a central carbon atom, which is bonded to two tert-butyl groups and two ethyl groups.
Derivative
It is a derivative of the widely used industrial solvent tetrachloroethylene.
Potential applications
It has potential applications in the fields of organic synthesis and materials science.
Unique structure
Its unique structure and properties make it an interesting target for further study and potential applications in various industries.
Carboxylate groups
The compound has four carboxylate groups, which are important for its chemical reactivity and potential applications.
Tert-butyl groups
The presence of two tert-butyl groups contributes to the compound's steric hindrance and stability.
Ethyl groups
The two ethyl groups attached to the central carbon atom provide additional functionality and potential for further chemical modification.
Industrial relevance
As a derivative of tetrachloroethylene, 1,1-di-tert-butyl 2,3-diethyl propane-1,1,2,3-tetracarboxylate may have potential applications in the industrial sector, particularly in the development of new materials and synthetic processes.
Further study
The compound's unique structure and potential applications warrant further research to better understand its properties and explore its use in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 5467-28-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,6 and 7 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5467-28:
(6*5)+(5*4)+(4*6)+(3*7)+(2*2)+(1*8)=107
107 % 10 = 7
So 5467-28-7 is a valid CAS Registry Number.
5467-28-7Relevant academic research and scientific papers
Sakamoto, Midori,Kaneko, Tetsuya,Orito, Yuya,Shimoda, Yasushi,Nakajima, Makoto
, p. 452 - 460 (2019)
The Michael reaction of malonates with maleates afforded the corresponding adducts in high yields with high enantioselectivities (up to 98% enantiomeric excess (ee)) by using dilithium 3,3′-dichlorobinaphtholate as a catalyst. The obtained Michael adducts
Sakamoto, Midori,Kaneko, Tetsuya,Orito, Yuya,Nakajima, Makoto
, p. 2477 - 2480 (2016)
Lithium 3,3′-chlorobinaphtholate was found to catalyze the enantioselective Michael addition of a malonic ester to a maleic ester. High enantioselectivities (>90% ee) were observed, especially in the reactions of 2-alkylmalonic esters and maleic esters.
