Category: 5391-39-9

Synthetic Route of 5391-39-9, A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 5391-39-9, Name is 1-Acetylimidazolidin-2-one, molecular formula is C5H8N2O2. In a Patent£¬once mentioned of 5391-39-9

Imidazole and imidazoline derivatives and uses thereof

This invention is directed to novel imidazole and imidazoline derivatives which are selective agonists for cloned human alpha2 adrenergic receptors. This invention is also related to the use of these compounds for the treatment of any disease where modulation of the alpha2 receptors may be useful. The invention further provides for a pharmaceutical composition comprising a therapeutically effective amount of the above-defined compounds and a pharmaceutically acceptable carrier.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Synthetic Route of 5391-39-9. In my other articles, you can also check out more blogs about 5391-39-9

Reference£º
Imidazolidine – Wikipedia,
Imidazolidine | C3H8N2225 – PubChem

In heterogeneous catalysis, the catalyst is in a different phase from the reactants. Computed Properties of C5H8N2O2, At least one of the reactants interacts with the solid surface in a physical process called adsorption in such a way. 5391-39-9, name is 1-Acetylimidazolidin-2-one. In an article£¬Which mentioned a new discovery about 5391-39-9

Nitroimidazoles: Part XVI – Some 1-Methyl-4-nitro-5-substituted Imidazoles

Treatment of 1-methyl-4-nitro-5-chloroimidazole (3) with 5-membered lactames, e.g. imidazolidinones, oxazolidinone and thiazolidinone affords N-imidazolyl derivatives (4a-d).Reaction of 3 with imidazole yields 4e; amino derivatives (4f-h) are similarly obtained. 2-Hydroxypyrazine, 4-hydroxyquinazoline and 3,4,5-trichlorophenol and 3 react to form O-derivatives (4i-k).Imidazole (11) is formed from 1-methyl-4-chloro-5-nitroimidazole (10).

I hope this article can help some friends in scientific research. I am very proud of our efforts over the past few months and hope to 5391-39-9, help many people in the next few years.Computed Properties of C5H8N2O2

Reference£º
Imidazolidine – Wikipedia,
Imidazolidine | C3H8N2229 – PubChem

Chemistry is traditionally divided into organic and inorganic chemistry. SDS of cas: 5391-39-9, The former is the study of compounds containing at least one carbon-hydrogen bonds.In a patent£¬Which mentioned a new discovery about 5391-39-9

Penicillins

Penicillins of the formula EQU1 or pharmaceutically acceptable non-toxic salts thereof, wherein C* is a carbon atom constituting a center of chirality; A is a moiety of the formula EQU2 or EQU3 wherein X is EQU4 Y is EQU5 or wherein Aryl is an aryl moiety; Z is EQU6 Q1 is EQU7 or SPC1 Q2 is EQU8 SPC2 or SPC3 R is straight- chain or branched alkyl of 1 to 5 carbon atoms; R1 is alkyl of 1 to 10 carbon atoms, cycloalkyl of 3 to 10 carbon atoms, alkenyl of 2 to 10 carbon atoms, cycloalkenyl of 3 to 10 carbon atoms. vinyl, arylvinyl, mono-, di-, or tri-halo-lower alkyl, H2 N–, R–NH–, (R)2 N–, aryl–NH–, aryl-lower alkylamino, alkoxy of 1 to 8 carbon atoms, aralkoxy of 1 to 8 carbon atoms in the alkoxy portion, cycloalkoxy of 3 to 7 carbon atoms, aryloxy, R–O–V–, R–S–V–, N=C–V–, R–O–CO–V–, H2 N–CO–V–, R–NH–CO–V–, R–O–CO–NH–, R–SO2 –NH–, (R)2 N–CO–V–, wherein R is as above defined, SPC4 SPC5 provided that when X is –SO2 –, R1 is not alkoxy, aralkoxy, cycloalkoxy or aryloxy, and further provided that R1 can also be hydrogen when X is –CO–; V is a divalent organic radical of 1 to 3 carbon atoms; n is 0, 1 or 2; R2 and R3 are the same or different and are each hydrogen, alkyl of 1 to 8 carbon atoms, alkenyl of 2 to 8 carbon atoms, vinyl, allyl, propenyl, cycloalkyl of 3 to 6 carbon atoms, cycloalkenyl of 3 to 6 carbon atoms, mono-, di- or tri-halo lower alkyl or aryl; R4, r5 and R6 are the same or different and are each hydrogen, nitro, cyano, (R)2 N–, (R)2 N–CO–, R–CO–NH–, R–O–CO–, R–CO–O–, R–, R–O–, wherein R is as above defined, H2 N–SO2 –, chlorine, bromine, iodine, fluorine or trifluoromethyl; G is hydrogen or straight or branched chain alkyl of 1 to 5 carbon atoms; and B is a moiety of the formula SPC6 wherein R7, r8 and R9 are the same or different and are each hydrogen, halogen, nitro, hydroxy, R–, R–O–, R–S–, R–SO– , R–SO2 –, (R)2 N–, R–CO–NH–, or R–CO–O– , wherein R is as above defined; the arrow in the divalent linking group ?Q2 ? means that the linkage of two atoms by the free valencies of this group must take place as indicated by the arrow; exhibit activity against both Gram-positive and Gram-negative bacteria.

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Reference£º
Imidazolidine – Wikipedia,
Imidazolidine | C3H8N2210 – PubChem