23770-12-9 Usage
Heterocyclic compound
Contains a pyrrolidinone ring
1-methyl-5-phenyl-3-pyrrolidinone is a heterocyclic compound, meaning it has a ring structure containing more than one type of atom. In this case, the ring consists of four carbon atoms and one oxygen atom.
Pyrrolidinone ring
Five-membered ring
The pyrrolidinone ring is a five-membered ring, meaning it is composed of five atoms (four carbon and one oxygen) connected in a circular arrangement.
Building block in synthesis
Pharmaceutical and agrochemical products
1-methyl-5-phenyl-3-pyrrolidinone is commonly used as a building block or intermediate in the synthesis of various pharmaceuticals and agrochemicals, making it an essential component in the production of these products.
Potential therapeutic effects
Anti-inflammatory and analgesic
Research has been conducted on 1-methyl-5-phenyl-3-pyrrolidinone for its potential anti-inflammatory and analgesic (pain-relieving) effects, indicating its possible use in the treatment of various medical conditions.
Industrial applications
Solvent in polymer, resin, and coating production
1-methyl-5-phenyl-3-pyrrolidinone is also used as a solvent in various industrial applications, such as the production of polymers, resins, and coatings, highlighting its versatility and importance in the industrial sector.
Check Digit Verification of cas no
The CAS Registry Mumber 23770-12-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,7,7 and 0 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 23770-12:
(7*2)+(6*3)+(5*7)+(4*7)+(3*0)+(2*1)+(1*2)=99
99 % 10 = 9
So 23770-12-9 is a valid CAS Registry Number.
23770-12-9Relevant articles and documents
HETEROCYCLIZATION OF ACRYLOYLOXIRANES TO 3-HYDROXY-4-PIPERIDINONES AND 2-(α-HYDROXYALKYL)-3-PYRROLIDINONES IN THE REACTION WITH METHYLAMINE
Zvonok, A. M.,Biba, V. I.,Stanishevskii, L. S.
, p. 1113 - 1119 (2007/10/02)
3-Hydroxy-4-piperidinones and 2-(α-hydroxyalkyl)-3-pyrrolidinones were obtained by the reaction of acryloyloxiranes with methylamine.It is shown that the regiospecifity of the heterocyclization of the products of addition of methylamine to the double bond of the acryloyloxirane is determined by the substituents attached to the α- and β-carbon atoms of the epoxide ring.
