40061-31-2 Usage
Organic compound
It is an organic compound because it is primarily composed of carbon, hydrogen, and other elements such as nitrogen and oxygen.
Pyridine ring
The compound contains a pyridine ring, which is a six-membered aromatic ring with one nitrogen atom replacing one carbon atom.
Tolyl group
It also contains a tolyl group, which is a benzene ring with a methyl group attached to it.
Conjugated enone system
The compound has a conjugated enone system, which is a system of alternating double bonds and carbonyl groups that allows for the delocalization of electrons.
Potential applications
Medicinal chemistry and drug development 1-PYRIDIN-3-YL-2-P-TOLYL-ETHANE-1,2-DIONE has potential applications in the field of medicinal chemistry and drug development due to its unique structure and properties.
Biological activities
Anti-inflammatory and antioxidant properties The compound may exhibit biological activities such as anti-inflammatory and antioxidant properties, which could make it useful in the development of new medications.
Further research and experimentation
Necessary to fully understand properties and potential uses More research and experimentation are needed to fully understand the properties and potential uses of 1-PYRIDIN-3-YL-2-P-TOLYL-ETHANE-1,2-DIONE, as its structure and properties may lead to new discoveries and applications in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 40061-31-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,0,6 and 1 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 40061-31:
(7*4)+(6*0)+(5*0)+(4*6)+(3*1)+(2*3)+(1*1)=62
62 % 10 = 2
So 40061-31-2 is a valid CAS Registry Number.
InChI:InChI=1/C14H11NO2/c1-10-4-6-11(7-5-10)13(16)14(17)12-3-2-8-15-9-12/h2-9H,1H3
40061-31-2Relevant articles and documents
Electrochemical oxidation-induced benzyl C–H carbonylation for the synthesis of aromatic α-diketones
Tan, Yu-Fang,Chen, Yuan,Li, Rui-Xue,Guan, Zhi,He, Yan-Hong
supporting information, (2021/12/21)
Electrochemical oxidation-induced direct carbonylation of benzyl C–H bond for the synthesis of aromatic α-diketones is described. In this process, tetrabutylammonium iodide (nBu4NI) not only acts as an electrolyte, but its iodine anion is oxidized to an iodine radical at the anode, acting as a hydrogen atom transfer agent. The iodine radical extracts the benzyl hydrogen atom and causes the carbonylation of the benzyl position, where O2 in the air is used as an oxygen source.
Imidazole derivatives in the treatment of pain
-
, (2008/06/13)
Compounds of the formula SPC1 Wherein R1 represents lower alkyl, cycloalkyl or phenyl which is optionally substituted by halogen, lower alkyl or lower alkoxy, and one of the groups R2 and R3 represents phenyl which is optionally substituted by halogen, lower alkyl, hydroxy, lower alkoxy, lower alkylthio or lower alkylsulphonyl, and the other represents a 6-membered heteroaromatic radical containing 1 or 2 ring nitrogen atoms, their N-oxides and salts, with anti-inflammatory, antinociceptive and antipyretic activity, they are active ingredients of pharmaceutical compositions and can be used for the relief and removal of pain as well as for the treatment of rheumatic, arthritic and other inflammatory complaints; an illustrative example is 2-isopropyl-4(5)-(p-methoxyphenyl)-5(4)-3-pyridyl-imidazole.
