198209-31-3

Basic information

• Product Name: 2-BROMO-5-(2',5'-DIMETHYL) PYRROLIDYL PYRIDINE
• Synonyms: 2-BROMO-5-(2',5'-DIMETHYL) PYRROLIDYL PYRIDINE;22-BROMO-6-(2,5-DIMETHYL-1H-PYRROL-1-YL)PYRIDINE;2-Bromo-5-(2',5'-dimethyl-1-pyrrolidylpyridine;2-bromo-6-(2,5-dimethyl-1H-pyrrol-1-yl)Pyridine
• CAS NO: 198209-31-3
• Molecular Formula: C₁₁H₁₁BrN₂
• Molecular Weight: 255.15
• Mol File: 198209-31-3.mol
• Article Data: 10

Chemical Properties

• Melting Point: 104 °C
• Boiling Point: 357.1±42.0 °C(Predicted)
• Appearance: /
• Density: 1.40±0.1 g/cm3(Predicted)
• PKA: -3.43±0.70(Predicted)
• CAS DataBase Reference: 2-BROMO-5-(2',5'-DIMETHYL) PYRROLIDYL PYRIDINE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-BROMO-5-(2',5'-DIMETHYL) PYRROLIDYL PYRIDINE(198209-31-3)
• EPA Substance Registry System: 2-BROMO-5-(2',5'-DIMETHYL) PYRROLIDYL PYRIDINE(198209-31-3)

Safety Data

• Hazardous Substances Data: 198209-31-3(Hazardous Substances Data)

Usage

General Description

2-BROMO-5-(2',5'-DIMETHYL) PYRROLIDYL PYRIDINE is a chemical compound containing a pyrrolidyl pyridine ring with a bromine substitution at the 2-position and two methyl groups at the 2' and 5' positions. It is commonly used as an intermediate in the synthesis of pharmaceutical compounds and agrochemicals. This chemical is also known to exhibit biological activity, making it a potential candidate for drug development and research. However, its exact applications and properties have not been extensively studied and documented, so further research and analysis are needed to fully understand the potential uses and effects of this compound.

Upstream product

• 19798-81-3 2-Amino-6-bromopyridine 
• 110-13-4 2,5-hexanedione 

Downstream Products

• 198209-33-5 2-(2,5-dimethylpyrrol-1-yl)-6-(4-(2-chloroethyl)phenyl)-pyridine 
• 251453-93-7 2-(2,5-dimethylpyrrolyl)-6-[4-benzyloxybicyclo[2.2.1]naphthalen-1-yl]pyridine 
• 221087-87-2 2-(2,5-dimethylpyrrolyl)-6-[4-benzyloxy-5,6,7,8-tetrahydronaphthalen-1-yl]pyridine 
• 675845-93-9 2-(2,5-dimethylpyrrolyl)-6-[4-benzyloxyindan-1-yl]pyridine 
• 221087-65-6 2-(2,5-dimethylpyrrolyl)-6-(4-benzyloxy-1-naphthyl)pyridine 
• 762275-96-7 2-(4-benzyloxy-5-t-butyldimethylsilyloxy-2-methoxy-phenyl)-6-(2,5-dimethyl-pyrrol-1-yl)-pyridine 
• 511277-71-7 2-(4-benzyloxy-5-ethyl-2-methoxy-phenyl)-6-(2,5-dimethyl-pyrrol-1-yl)-pyridine 
• 762275-75-2 2-(2,5-dimethyl-pyrrol-1-yl)-6-(4-[1,3]dioxolan-2-yl-2,5-dimethoxy-phenyl)-pyridine 
• 956384-73-9 4,6'-diamino-2,2'-bipyridine 

Relevant articles and documents

Synthesis of diisothiocyanato-functionalized 2,2-bipyridines

Three new diisothiocyanato-functionalized 2,2-bipyridines have been synthesized in four consecutive steps. Starting from 4-amino-2-chloro- and 2-amino-6-bromopyridine, respectively, we first prepared the corresponding diamino-2,2-bipyridines via homo- or Negishi cross-coupling reactions which were subsequently reacted with thiophosgene.

Towards allosteric receptors synthesis of β-cyclodextrin- functionalised 2,2'-bipyridines and their metal complexes

Herein, we present three new 2,2'-bipyridines that carry two β-cyclodextrin moieties in different substitution patterns. When coordinated by zinc(II) or copper(I) ions (or their complexes), these compounds undergo conformational changes and switch between

Synthesis of substituted 2,2′-bipyridines from 2-bromo- or 2-chloropyridines using tetrakis(triphenylphosphine)palladium(0) as a catalyst in a modified Negishi cross-coupling reaction

A protocol for an efficient, modified Negishi cross-coupling strategy for substituted 2,2′-bipyridines employing tetrakis(triphenylphosphine) palladium(0) as a simple, commercially available, and relatively inexpensive catalyst for both 2-bromo- and 2-chl