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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=NC=CC=C1

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

Unknown
149124
PubMed

PubMed

TitleDatePubMed
Synthesis and characterization of aryl substituted bis(2-pyridyl)amines and their copper olefin complexes: investigation of remote steric control over olefin binding.
2010-12-21
2-Hydroxypyridine photolytic degradation by 254 nm UV irradiation at different conditions.
2009-11
Photolytic removal and mineralisation of 2-halogenated pyridines.
2009-09
Deprotonative magnesation and cadmation of [1,2,3]triazolo[1,5-a]pyridines.
2009-01-02
Bis(2-bromo-pyridinium) hexa-bromido-stannate(IV).
2008-05-03
Bis(2-bromo-pyridinium) hexa-chlorido-stannate(IV).
2008-04-10
A concise synthesis of lentiginosine derivatives using a pyridinium formation via the Mitsunobu reaction.
2008-02-01
Concise total synthesis of the thiazolyl peptide antibiotic GE2270 A.
2008
Study on reaction kinetics of synthesis of thioether by a visualization technique.
2007-09-01
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.
2007-02-15
Regioselective synthesis of bis(2-halo-3-pyridyl) dichalcogenides (E = S, Se and Te): directed ortho-lithiation of 2-halopyridines.
2007
Synthesis and characterisation of eight isomeric bis(2-pyridyloxy)naphthalenes.
2006-09-13
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.
2005-12-23
Improved synthesis of aryltrialkoxysilanes via treatment of aryl Grignard or lithium reagents with tetraalkyl orthosilicates.
2004-11-26
A new totally flat N(sp(2))C(sp(2))N(sp(2)) pincer palladacycle: synthesis and photoluminescent properties.
2004-01-26
Siloxane-based cross-coupling of bromopyridine derivatives: studies for the synthesis of streptonigrin and lavendamycin.
2003-12-11
Electrophilic terminal phosphinidene complex-Lewis base adducts: chemistry between carbon-halide bond activation and weak Lewis base adduct formation.
2003-12-07
Combined application of organozinc chemistry and one-pot hydroboration-Suzuki coupling to the synthesis of amino acids.
2003-03-21
Electrochemical homocoupling of 2-bromomethylpyridines catalyzed by nickel complexes.
2002-03-22
Directed deprotonation-transmetalation as a route to substituted pyridines.
2001-03-22
Patents

Patents

04064254
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04180670
3
04195088
1
04372953
14
04547506
5
04622326
1
04927838
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04994087
1
05070087
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05202326
1
05272147
1
05346906
1
05426107
1
05466698
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05512575
32
05616585
1
05780482
1
05861421
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06166006
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06235730
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06372736
3
06387911
2
06455720
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06458849
5
06462092
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06534510
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06677380
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06696435
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06696472
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06962783
1
07176204
1
07262185
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07285666
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07326788
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07456164
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07504412
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07542196
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07544704
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07566781
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07635527
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07642367
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07666879
13
07736757
2
07777050
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07795236
2
07807671
1
07807676
2
07834021
1
07851636
6
Substance Class Chemical
Created
by admin
on Mon Mar 31 17:34:47 GMT 2025
Edited
by admin
on Mon Mar 31 17:34:47 GMT 2025
Record UNII
7Z7MLC4VD8
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NSC-8031
Preferred Name English
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
PYRIDINE, 2-BROMO-
Systematic Name English
2-BROMOPYRIDIN
Systematic Name English
Code System Code Type Description
NSC
8031
Created by admin on Mon Mar 31 17:34:47 GMT 2025 , Edited by admin on Mon Mar 31 17:34:47 GMT 2025
PRIMARY
CHEBI
51574
Created by admin on Mon Mar 31 17:34:47 GMT 2025 , Edited by admin on Mon Mar 31 17:34:47 GMT 2025
PRIMARY
PUBCHEM
7973
Created by admin on Mon Mar 31 17:34:47 GMT 2025 , Edited by admin on Mon Mar 31 17:34:47 GMT 2025
PRIMARY
WIKIPEDIA
2-Bromopyridine
Created by admin on Mon Mar 31 17:34:47 GMT 2025 , Edited by admin on Mon Mar 31 17:34:47 GMT 2025
PRIMARY
CAS
109-04-6
Created by admin on Mon Mar 31 17:34:47 GMT 2025 , Edited by admin on Mon Mar 31 17:34:47 GMT 2025
PRIMARY
FDA UNII
7Z7MLC4VD8
Created by admin on Mon Mar 31 17:34:47 GMT 2025 , Edited by admin on Mon Mar 31 17:34:47 GMT 2025
PRIMARY
EPA CompTox
DTXSID6051564
Created by admin on Mon Mar 31 17:34:47 GMT 2025 , Edited by admin on Mon Mar 31 17:34:47 GMT 2025
PRIMARY
ECHA (EC/EINECS)
203-641-6
Created by admin on Mon Mar 31 17:34:47 GMT 2025 , Edited by admin on Mon Mar 31 17:34:47 GMT 2025
PRIMARY
NIH
NCATS
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