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Details

Stereochemistry ACHIRAL
Molecular Formula C5H4BrN
Molecular Weight 157.996
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 3-BROMOPYRIDINE

SMILES

BrC1=CN=CC=C1

InChI

InChIKey=NYPYPOZNGOXYSU-UHFFFAOYSA-N
InChI=1S/C5H4BrN/c6-5-2-1-3-7-4-5/h1-4H

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Mechanistic insights into a gas-solid reaction in molecular crystals: the role of hydrogen bonding.
2010-11-15
catena-Poly[[bis-(μ-5-bromo-pyridine-3-carboxyl-ato-κO:O')dicopper(II)]-bis-(μ-5-bromo-pyridine-3-carboxyl-ato)-κO,O':N;κN:O,O'].
2010-10-23
2-(6-Bromo-3-pyrid-yl)-8-methyl-imidazo[1,2-a]pyrazine.
2010-06-23
Synthesis and crossover reaction of TEMPO containing block copolymer via ROMP.
2010-06-01
Synthesis, structural characterization and photoluminescence properties of rhenium(I) complexes based on bipyridine derivatives with carbazole moieties.
2009-12-21
Structure-activity relationships of heteroaromatic esters as human rhinovirus 3C protease inhibitors.
2009-07-01
Synthetic mimic of antimicrobial peptide with nonmembrane-disrupting antibacterial properties.
2008-11
Aryl methylene ketones and fluorinated methylene ketones as reversible inhibitors for severe acute respiratory syndrome (SARS) 3C-like proteinase.
2008-10
Synthesis of Novel 3-Aryl-N-Methyl-1,2,5,6-Tetrahydropyridine Derivatives by Suzuki coupling: As Acetyl Cholinesterase Inhibitors.
2007-09-05
Rate-determining cooperative effects of bimolecular reactions in solution.
2006-12-14
The fate of platinum(II) and platinum(IV) anti-cancer agents in cancer cells and tumours.
2006-07
Synthesis and reactivity of some 6-substituted-2,4-dimethyl-3-pyridinols, a novel class of chain-breaking antioxidants.
2004-12-24
A facile synthesis of cis-1-methyl-1,2,3,3a,4,8b- hexahydropyrrolo[3,2-f]pyrindine, an annulated nicotine analog.
2002-12-12
An improved protocol for the preparation of 3-pyridyl- and some arylboronic acids.
2002-07-26
Synthesis of (+/-)-methyl-(1-aryl-4-pyridin-3-yl-but-3-enyl)-amines.
2001-12
Directed deprotonation-transmetalation as a route to substituted pyridines.
2001-03-22
Patents
Name Type Language
NSC-3974
Preferred Name English
3-BROMOPYRIDINE
Systematic Name English
PYRIDINE, 3-BROMO-
Systematic Name English
M-BROMOPYRIDINE
Systematic Name English
5-BROMOPYRIDINE
Systematic Name English
PYRIDIN-3-YL BROMIDE
Systematic Name English
3-PYRIDYL BROMIDE
Systematic Name English
Code System Code Type Description
EPA CompTox
DTXSID9060819
Created by admin on Mon Mar 31 19:22:51 GMT 2025 , Edited by admin on Mon Mar 31 19:22:51 GMT 2025
PRIMARY
ECHA (EC/EINECS)
210-952-0
Created by admin on Mon Mar 31 19:22:51 GMT 2025 , Edited by admin on Mon Mar 31 19:22:51 GMT 2025
PRIMARY
CAS
626-55-1
Created by admin on Mon Mar 31 19:22:51 GMT 2025 , Edited by admin on Mon Mar 31 19:22:51 GMT 2025
PRIMARY
PUBCHEM
12286
Created by admin on Mon Mar 31 19:22:51 GMT 2025 , Edited by admin on Mon Mar 31 19:22:51 GMT 2025
PRIMARY
CHEBI
51575
Created by admin on Mon Mar 31 19:22:51 GMT 2025 , Edited by admin on Mon Mar 31 19:22:51 GMT 2025
PRIMARY
FDA UNII
XMN8H2XE9H
Created by admin on Mon Mar 31 19:22:51 GMT 2025 , Edited by admin on Mon Mar 31 19:22:51 GMT 2025
PRIMARY
WIKIPEDIA
3-Bromopyridine
Created by admin on Mon Mar 31 19:22:51 GMT 2025 , Edited by admin on Mon Mar 31 19:22:51 GMT 2025
PRIMARY
NSC
3974
Created by admin on Mon Mar 31 19:22:51 GMT 2025 , Edited by admin on Mon Mar 31 19:22:51 GMT 2025
PRIMARY