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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 2-BROMOPYRIDINE

SMILES

BrC1=CC=CC=N1

InChI

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

HIDE SMILES / InChI

Molecular Formula C5H4BrN
Molecular Weight 157.996
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Directed deprotonation-transmetalation as a route to substituted pyridines.
2001 Mar 22
Electrochemical homocoupling of 2-bromomethylpyridines catalyzed by nickel complexes.
2002 Mar 22
Siloxane-based cross-coupling of bromopyridine derivatives: studies for the synthesis of streptonigrin and lavendamycin.
2003 Dec 11
Electrophilic terminal phosphinidene complex-Lewis base adducts: chemistry between carbon-halide bond activation and weak Lewis base adduct formation.
2003 Dec 7
Combined application of organozinc chemistry and one-pot hydroboration-Suzuki coupling to the synthesis of amino acids.
2003 Mar 21
A new totally flat N(sp(2))C(sp(2))N(sp(2)) pincer palladacycle: synthesis and photoluminescent properties.
2004 Jan 26
Improved synthesis of aryltrialkoxysilanes via treatment of aryl Grignard or lithium reagents with tetraalkyl orthosilicates.
2004 Nov 26
Mixed effect of the supporting electrolyte and the zinc anode in the electrochemical homocoupling of 2-bromopyridines catalyzed by nickel complexes in an undivided cell.
2005 Dec 23
Synthesis and characterisation of eight isomeric bis(2-pyridyloxy)naphthalenes.
2006 Sep 13
Regioselective synthesis of bis(2-halo-3-pyridyl) dichalcogenides (E = S, Se and Te): directed ortho-lithiation of 2-halopyridines.
2007
Synthesis and antioxidant activity evaluation of new 7-aryl or 7-heteroarylamino-2,3-dimethylbenzo[b]thiophenes obtained by Buchwald-Hartwig C-N cross-coupling.
2007 Feb 15
Study on reaction kinetics of synthesis of thioether by a visualization technique.
2007 Sep 1
Concise total synthesis of the thiazolyl peptide antibiotic GE2270 A.
2008
Bis(2-bromo-pyridinium) hexa-chlorido-stannate(IV).
2008 Apr 10
A concise synthesis of lentiginosine derivatives using a pyridinium formation via the Mitsunobu reaction.
2008 Feb 1
Bis(2-bromo-pyridinium) hexa-bromido-stannate(IV).
2008 May 3
Deprotonative magnesation and cadmation of [1,2,3]triazolo[1,5-a]pyridines.
2009 Jan 2
2-Hydroxypyridine photolytic degradation by 254 nm UV irradiation at different conditions.
2009 Nov
Photolytic removal and mineralisation of 2-halogenated pyridines.
2009 Sep
Synthesis and characterization of aryl substituted bis(2-pyridyl)amines and their copper olefin complexes: investigation of remote steric control over olefin binding.
2010 Dec 21
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:00:16 GMT 2023
Edited
by admin
on Fri Dec 15 15:00:16 GMT 2023
Record UNII
7Z7MLC4VD8
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2-BROMOPYRIDINE
Systematic Name English
.BETA.-BROMOPYRIDINE
Systematic Name English
O-BROMOPYRIDINE
Systematic Name English
PYRIDIN-2-YL BROMIDE
Systematic Name English
2-PYRIDYL BROMIDE
Systematic Name English
NSC-8031
Code English
PYRIDINE, 2-BROMO-
Systematic Name English
2-BROMOPYRIDIN
Systematic Name English
Code System Code Type Description
NSC
8031
Created by admin on Fri Dec 15 15:00:16 GMT 2023 , Edited by admin on Fri Dec 15 15:00:16 GMT 2023
PRIMARY
CHEBI
51574
Created by admin on Fri Dec 15 15:00:16 GMT 2023 , Edited by admin on Fri Dec 15 15:00:16 GMT 2023
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PUBCHEM
7973
Created by admin on Fri Dec 15 15:00:16 GMT 2023 , Edited by admin on Fri Dec 15 15:00:16 GMT 2023
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WIKIPEDIA
2-Bromopyridine
Created by admin on Fri Dec 15 15:00:16 GMT 2023 , Edited by admin on Fri Dec 15 15:00:16 GMT 2023
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CAS
109-04-6
Created by admin on Fri Dec 15 15:00:16 GMT 2023 , Edited by admin on Fri Dec 15 15:00:16 GMT 2023
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FDA UNII
7Z7MLC4VD8
Created by admin on Fri Dec 15 15:00:16 GMT 2023 , Edited by admin on Fri Dec 15 15:00:16 GMT 2023
PRIMARY
EPA CompTox
DTXSID6051564
Created by admin on Fri Dec 15 15:00:16 GMT 2023 , Edited by admin on Fri Dec 15 15:00:16 GMT 2023
PRIMARY
ECHA (EC/EINECS)
203-641-6
Created by admin on Fri Dec 15 15:00:16 GMT 2023 , Edited by admin on Fri Dec 15 15:00:16 GMT 2023
PRIMARY