107812-86-2 Usage
Uses
Used in Pharmaceutical Industry:
3-ethyl 5-methyl 2-(chloromethyl)-4-(2-chlorophenyl)-1,4-dihydro-6-methylpyridine-3,5-dicarboxylate is used as a potential pharmaceutical agent for its possible biological activity. The molecule's functional groups may contribute to its pharmacological properties, making it a candidate for the development of new drugs or therapeutic agents.
Used in Organic Synthesis:
In the field of organic chemistry, 3-ethyl 5-methyl 2-(chloromethyl)-4-(2-chlorophenyl)-1,4-dihydro-6-methylpyridine-3,5-dicarboxylate serves as a valuable precursor for the synthesis of other organic compounds. Its unique structure and functional groups can be utilized in the creation of novel molecules with specific applications in various industries.
Used in Medicinal Chemistry Research:
3-ethyl 5-methyl 2-(chloromethyl)-4-(2-chlorophenyl)-1,4-dihydro-6-methylpyridine-3,5-dicarboxylate is employed as a subject of study in medicinal chemistry research. Its complex structure and potential biological activity make it an interesting target for investigations into new drug discovery and the understanding of molecular interactions with biological systems.
Check Digit Verification of cas no
The CAS Registry Mumber 107812-86-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,8,1 and 2 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 107812-86:
(8*1)+(7*0)+(6*7)+(5*8)+(4*1)+(3*2)+(2*8)+(1*6)=122
122 % 10 = 2
So 107812-86-2 is a valid CAS Registry Number.
107812-86-2Relevant academic research and scientific papers
Synthesis of unsymmetrical 1, 4-dihydropyridine derivatives in ionic liquid and inference on the formation mechanism of furopyridines
Zhang, Jian,Jin, Long Fei
, p. 916 - 921 (2012/02/16)
Aromatic aldehydes, methyl acetoacetate, ethyl acetoacetate, ammonium acetate, ethyl 4-chloroacetoacetate as materials, eight unsymmetrical 1, 4-dihydropyridine derivatives were synthesized in ionic liquid [Bmim]OH in short time with the 60%-90% yield, and the ionic liquid could be utilized for 5 times repeatedly with the no decrease of the yield, four of products [3(a-d)] (see in Table-1) were synthesized through Knoevenagel and Michael addition reaction, and another four Furopyridines [3(e-h)] (see in Table-2) through one-pot synthesis whose formation mechanism being different from that of [3(a-d)] was first inferred.
