257937-23-8 Usage
Description
3-Bromo-4-(pyrrolidin-1-yl)pyridine is a pyridine derivative with the molecular formula C10H12BrN2. It features a bromine atom at the 3-position and a pyrrolidin-1-yl group at the 4-position, making it a valuable building block in pharmaceutical research and organic synthesis.
Uses
Used in Pharmaceutical Research:
3-Bromo-4-(pyrrolidin-1-yl)pyridine is used as a building block for the synthesis of various chemical compounds and pharmaceutical drugs. Its unique structure allows for the development of new drugs with potential therapeutic applications.
Used in Organic Synthesis:
As a reagent, 3-Bromo-4-(pyrrolidin-1-yl)pyridine is utilized in organic synthesis to create a range of chemical products, contributing to the advancement of chemical research and industry.
Used in Coordination Chemistry:
3-Bromo-4-(pyrrolidin-1-yl)pyridine also serves as a ligand in coordination chemistry, playing a crucial role in the formation and stabilization of metal complexes.
Used in Drug Development:
With its potential applications in the development of new drugs and materials, 3-Bromo-4-(pyrrolidin-1-yl)pyridine is an important component in the ongoing pursuit of innovative pharmaceutical solutions.
It is important to handle 3-Bromo-4-(pyrrolidin-1-yl)pyridine with care due to its potential health and environmental hazards if not properly managed.
Check Digit Verification of cas no
The CAS Registry Mumber 257937-23-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,7,9,3 and 7 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 257937-23:
(8*2)+(7*5)+(6*7)+(5*9)+(4*3)+(3*7)+(2*2)+(1*3)=178
178 % 10 = 8
So 257937-23-8 is a valid CAS Registry Number.
257937-23-8Relevant articles and documents
Single-Handed Helical Poly(quinoxaline-2,3-diyl)s Bearing Achiral 4-Aminopyrid-3-yl Pendants as Highly Enantioselective, Reusable Chiral Nucleophilic Organocatalysts in the Steglich Reaction
Yamamoto, Takeshi,Murakami, Ryo,Suginome, Michinori
supporting information, p. 2557 - 2560 (2017/03/01)
Helically chiral poly(quinoxaline-2,3-diyl)s bearing 4-aminopyrid-3-yl pendants were synthesized as new helical-polymer-based chiral nucleophilic organocatalysts. The obtained chiral nucleophilic polymer catalysts exhibited high catalytic activity, enantioselectivity, and reusability in asymmetric Steglich rearrangement of oxazolyl carbonate to C-carboxyazlactone. The polyquinoxaline-based, helically chiral DMAP catalyst mediated intramolecular acyl transfer selectively, by contrast with known small-molecule-based chiral organocatalysts, which also mediate intermolecular acyl transfers.
