60026-17-7 Usage
Description
1-(3-methylbutyl)pyrrolidine, also known as MPB, is a chemical compound characterized by the presence of a pyrrolidine ring attached to a 3-methylbutyl group. This versatile molecule is recognized for its potential antioxidant and anti-inflammatory properties, positioning it as a promising candidate for the development of therapeutic agents targeting a range of conditions. Furthermore, MPB's utility extends to the synthesis of biologically active compounds, including those with antiviral and antibacterial properties, showcasing its value in pharmaceutical research and organic synthesis.
Uses
Used in Pharmaceutical Research:
1-(3-methylbutyl)pyrrolidine is used as a building block for the development of therapeutic agents due to its potential antioxidant and anti-inflammatory properties. These characteristics make MPB a valuable candidate for creating medications aimed at treating various conditions that benefit from these effects.
Used in Organic Synthesis:
In the field of organic synthesis, 1-(3-methylbutyl)pyrrolidine is utilized as a key component in the creation of other compounds with biological activity. Its structural features facilitate the synthesis of a diverse array of molecules, contributing to the advancement of chemical research and the development of new pharmaceuticals.
Used in Antiviral and Antibacterial Agents:
MPB is also employed in the synthesis of compounds with antiviral and antibacterial properties. Its incorporation into these agents enhances their effectiveness against a variety of pathogens, making it a crucial component in the fight against infectious diseases.
Overall, 1-(3-methylbutyl)pyrrolidine is a multifaceted chemical with applications spanning across pharmaceutical research, organic synthesis, and the development of therapeutic agents for various medical conditions. Its versatility and potential for further investigation make it an essential tool in the ongoing pursuit of innovative treatments and pharmaceutical advancements.
Check Digit Verification of cas no
The CAS Registry Mumber 60026-17-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,0,2 and 6 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 60026-17:
(7*6)+(6*0)+(5*0)+(4*2)+(3*6)+(2*1)+(1*7)=77
77 % 10 = 7
So 60026-17-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H17NO/c1-8(2)7-9(11)10-5-3-4-6-10/h8H,3-7H2,1-2H3
60026-17-7Relevant articles and documents
Chemoselective Intermolecular Cross-Enolate-Type Coupling of Amides
Kaiser, Daniel,Teskey, Christopher J.,Adler, Pauline,Maulide, Nuno
supporting information, p. 16040 - 16043 (2017/11/22)
A new approach for the synthesis of 1,4-dicarbonyl compounds is reported. Chemoselective activation of amide carbonyl functionality and subsequent umpolung via N-oxide addition generates an electrophilic enolonium species that can be coupled with a wide range of nucleophilic enolates. The method conveys broad functional group tolerance on both components, does not suffer from formation of homocoupling byproducts and avoids the use of transition metal catalysts.
Chemoselective intermolecular α-arylation of amides
Peng, Bo,Geerdink, Danny,Fares, Christophe,Maulide, Nuno
supporting information, p. 5462 - 5466 (2014/06/09)
A new approach for the fully chemoselective α-arylation of amides is presented. By means of electrophilic amide activation, aryl groups can be regioselectively introduced α- to amides, even in the presence of esters and alkyl ketones. Mechanistic studies reveal key reaction intermediates and emphasize a remarkably subtle base effect in this transformation. Arylating me softly: A new approach for the fully chemoselective α-arylation of amides has been developed. When electrophilic amide activation is employed, aryl groups can be regioselectively introduced in the position α to the amide, and that even in the presence of esters or alkyl ketones. Mechanistic studies emphasize a remarkably subtle base effect in this transformation.
Gold-catalyzed amide synthesis from aldehydes and amines in aqueous medium
Li, Gai-Li,Kung, Karen Ka-Yan,Wong, Man-Kin
supporting information; experimental part, p. 4112 - 4114 (2012/06/16)
An efficient gold-catalyzed amide synthesis from aldehydes and amines in aqueous medium under mild reaction conditions has been developed.
