39101-27-4 Usage
Description
1-(2-nitrobenzyl)pyrrolidine-2,5-dione is a chemical compound characterized by its molecular formula C14H13NO4. It is a white to off-white powder that is prominently utilized in the realms of organic synthesis and medicinal chemistry. 1-(2-nitrobenzyl)pyrrolidine-2,5-dione is distinguished by its pyrrolidine-2,5-dione ring, which is substituted with a 2-nitrobenzyl group. This unique structure renders it a valuable asset in the creation of pharmaceuticals and agrochemicals. Furthermore, it serves as an intermediate in the synthesis of a variety of biologically active compounds. The nitro group present in the compound enhances its versatility as a building block for the preparation of diverse molecules with potential pharmacological and biological activity.
Uses
Used in Pharmaceutical Industry:
1-(2-nitrobenzyl)pyrrolidine-2,5-dione is used as a key intermediate for the development of pharmaceuticals due to its unique structure and the presence of the nitro group. This allows for the creation of a wide range of biologically active compounds with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical industry, 1-(2-nitrobenzyl)pyrrolidine-2,5-dione is utilized as a building block for the synthesis of various agrochemicals. Its unique structure and functional groups contribute to the development of effective compounds for agricultural use.
Used in Organic Synthesis:
1-(2-nitrobenzyl)pyrrolidine-2,5-dione is employed as a versatile intermediate in organic synthesis. The presence of the nitro group makes it a valuable building block for the preparation of a diverse array of molecules with potential applications in various fields, including pharmaceuticals, agrochemicals, and other industries.
Used in the Synthesis of Biologically Active Compounds:
This chemical compound is used as a starting material for the synthesis of biologically active compounds. The unique structure and functional groups of 1-(2-nitrobenzyl)pyrrolidine-2,5-dione make it an ideal candidate for the development of new molecules with potential pharmacological and biological activities.
Check Digit Verification of cas no
The CAS Registry Mumber 39101-27-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,1,0 and 1 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 39101-27:
(7*3)+(6*9)+(5*1)+(4*0)+(3*1)+(2*2)+(1*7)=94
94 % 10 = 4
So 39101-27-4 is a valid CAS Registry Number.
39101-27-4Relevant articles and documents
Electrochemical reduction of N-(o-nitrobenzoyl) and N-(o-nitrobenzyl)-amides or imides. Electrosynthesis of quinazoline derivatives.
Chibani, A.,Hazard, R.,Tallec, A.
, p. 814 - 822 (2007/10/02)
Controlled potential electrolysis at a mercury pool cathode, carried out at the plateau of the first reduction wave of o-nitrobenzoylacetamide, leads to 4-hydroxy-2-methylquinazoline 1-oxide, resulting from a ring closure of the phenylhydroxylamine intermediate.In the same conditions, o-nitrobenzoylsuccinimide gives rise to a tricyclic compound which undergoes a nucleophilic attack from the electrolysis medium, with formation of 4-hydroxyquinazoline 1-oxide bearing at the position 2, either a propanoate group (acidic media) or a propanamido group (ammoniacal buffer).At last, the hydroxylamino derivative issued from o-nitrobenzoyl- phtalimide reduction, disproportionates in acidic medium and a mixture of 2-(o-carboxyphenyl)-4-hydroxyquinazoline 1-oxide and of the parent quinazoline is obtained at the term of the electrolysis.As a matter of comparison, the parent o-nitrobenzyl substrates have been studied; no ring closure occurs at the hydroxylamino stage but quinazoline derivatives can be obtained from the corresponding anilines by electroreduction at more negative potentials. Key words: polarography / cyclic voltammetry / controlled potential electrolysis / quinazoline 1-oxyde / quinazoline
