38167-72-5 Usage
Uses
Used in Organic Synthesis:
N-(2,6-Diethylphenyl)maleimide is used as a dienophile in Diels-Alder reactions for the synthesis of various organic compounds. Its reactivity and stability make it a versatile compound in this field.
Used in Polymer Production:
DEPMI is utilized in the production of polymers due to its ability to participate in Diels-Alder reactions, which can lead to the formation of polymers with specific properties.
Used in Pharmaceutical Industry:
N-(2,6-Diethylphenyl)maleimide is used in the pharmaceutical industry for the synthesis of various drugs. Its reactivity and stability contribute to the development of new pharmaceutical compounds.
Used in Agrochemicals:
DEPMI is also employed in the production of agrochemicals, where its properties can be harnessed to create effective and stable products for agricultural applications.
It is important to handle and store N-(2,6-Diethylphenyl)maleimide with care, as it can be hazardous if not properly managed.
Check Digit Verification of cas no
The CAS Registry Mumber 38167-72-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,1,6 and 7 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 38167-72:
(7*3)+(6*8)+(5*1)+(4*6)+(3*7)+(2*7)+(1*2)=135
135 % 10 = 5
So 38167-72-5 is a valid CAS Registry Number.
InChI:InChI=1/C14H15NO2/c1-3-10-6-5-7-11(4-2)14(10)15-12(16)8-9-13(15)17/h5-9H,3-4H2,1-2H3
38167-72-5Relevant academic research and scientific papers
Unusual regio- and stereo-selectivity in Diels-Alder reactions between bulky N-phenylmaleimides and anthracene derivatives
Chen, Hao,Yao, Erdong,Xu, Chi,Meng, Xiao,Ma, Yuguo
, p. 5102 - 5107 (2014/07/08)
Unusual regio- and stereo-selectivity in Diels-Alder (D-A) reactions were achieved between bulky N-phenylmaleimides and anthracene derivatives. Using multiple substituents with steric hindrance on both diene and dienophile, a noticeable shift toward 1,4-addition was successfully obtained. The substrate scope in this reaction was broad and the highest yield of anti-1,4-adducts was over 90%. Novel structures of anti-1,4-adducts were confirmed by single crystal X-ray diffraction analysis. This study not only provides the first reported method of synthesizing anti-1,4-adducts and achieving otherwise unattainable regio- and stereo-selectivity, but also elucidates the importance of combining the steric effects of two reactants to shift products toward 1,4-adducts. Moreover, the resulting 1,4-adducts could be further functionalized through their halogen groups via carbon-carbon coupling reactions.
Xn:Harmful;
