ChemicalBook > CAS DataBase List > 2-Bromopyridine

2-Bromopyridine

Product Name
2-Bromopyridine
CAS No.
109-04-6
Chemical Name
2-Bromopyridine
Synonyms
-Bromopyridine;-Bromoazine;2-Brompyridin;2-Bromopyridine;2-bromo-pyridin;o-Bromopyridine;2-pyridylbromide;AKOS BBS-00004324;BROMOPYRIDINE(2-);Pyridine,2-bromo-
CBNumber
CB3465833
Molecular Formula
C5H4BrN
Formula Weight
158
MOL File
109-04-6.mol
More
Less

2-Bromopyridine Property

Melting point:
193°C
Boiling point:
192-194 °C (lit.)
Density 
1.657 g/mL at 25 °C (lit.)
refractive index 
n20/D 1.572(lit.)
Flash point:
130 °F
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
solubility 
20g/l
form 
Liquid
pka
pK1: 0.71(+1) (25°C)
color 
Clear colorless to pale brown
Water Solubility 
Slightly miscible with water.
BRN 
105789
Dielectric constant
24.02
Stability:
Stable. Flammable. Incompatible with strong oxidizing agents, strong acids, acid chlorides.
InChIKey
IMRWILPUOVGIMU-UHFFFAOYSA-N
LogP
1.42
CAS DataBase Reference
109-04-6(CAS DataBase Reference)
NIST Chemistry Reference
Pyridine, 2-bromo-(109-04-6)
EPA Substance Registry System
Pyridine, 2-bromo- (109-04-6)
More
Less

Safety

Hazard Codes 
T,Xn,F
Risk Statements 
10-24/25-36/37/38-23/24/25-20/21/22
Safety Statements 
16-36/37-45-38-36/37/39-28A-26
RIDADR 
UN 2929 6.1/PG 2
WGK Germany 
3
RTECS 
US3850000
8
Hazard Note 
Toxic
TSCA 
Yes
HazardClass 
6.1
PackingGroup 
II
HS Code 
29333999
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Hazard statements

H301Toxic if swalloed

H310Fatal in contact with skin

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P262Do not get in eyes, on skin, or on clothing.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

More
Less

N-Bromosuccinimide Price

Sigma-Aldrich
Product number
B80100
Product name
2-Bromopyridine
Purity
99%
Packaging
25g
Price
$43.1
Updated
2024/03/01
Sigma-Aldrich
Product number
B80100
Product name
2-Bromopyridine
Purity
99%
Packaging
100g
Price
$123
Updated
2024/03/01
TCI Chemical
Product number
B0650
Product name
2-Bromopyridine
Purity
>98.0%(GC)
Packaging
25mL
Price
$53
Updated
2024/03/01
TCI Chemical
Product number
B0650
Product name
2-Bromopyridine
Purity
>98.0%(GC)
Packaging
100mL
Price
$146
Updated
2024/03/01
Alfa Aesar
Product number
A13241
Product name
2-Bromopyridine, 99%
Packaging
25g
Price
$41
Updated
2024/03/01
More
Less

2-Bromopyridine Chemical Properties,Usage,Production

Chemical Properties

light yellow oily or dark red liquid. miscible with ethanol, ether, benzene and pyridine, still soluble in water.

Uses

2-Bromopyridine is a 2-halogenated pyridine used in the preparation of a variety of biologically active compounds such as antimalarial agents and beta-adrenoceptor agonist.

Application

2-Bromopyridine can be used as:
A building block in the formation of C?N bond by various cross coupling reactions.
A reactant in Negishi cross-coupling reaction with aryl halides catalyzed by palladium.
A reactant in the synthesis of 2′-pyridyldifluoroacetate with ethyl bromodifluoroacetate in presence of copper as a catalyst.

Preparation

2-Bromopyridine is synthesized from 2-aminopyridine by bromination. In industrial production, hydrobromic acid (over 48%) is first cooled to below 0°C, 2-aminopyridine is slowly added, and then liquid bromine is added dropwise in a salt bath under freezing, and the rate of addition is to control the reaction temperature below -5°C appropriate. After adding, add sodium nitrite aqueous solution dropwise, control the reaction temperature to be below 0°C, stir for 20-30min, dropwise add 50% sodium hydroxide solution, extract the reaction solution with ether, wash with water, dry with anhydrous sodium sulfate, filter, and recover Diethyl ether, the residue was distilled under reduced pressure, and the 88°C-94°C/3333Pa fraction was collected to obtain the finished product of 2-bromopyridine with a yield of 83.8%.

Definition

ChEBI: 2-bromopyridine is a monobromopyridine.

Reactions

2-Bromopyridine reacts with butyllithium to give 2-lithiopyridine, which is a versatile reagent.Pyrithione can be prepared in a two-step synthesis from 2-bromopyridine by oxidation to the N-oxide with a suitable peracid followed by substitution using either sodium dithionite or sodium sulfide with sodium hydroxide to introduce the thiol functional group.

Flammability and Explosibility

Flammable

Purification Methods

Dry 2-bromopyridine over KOH for several days, then distil it from CaO under reduced pressure, and taking the middle fraction. [Beilstein 20/5 V 422.]

More
Less

2-Bromopyridine Suppliers

Pure Chemistry Scientific Inc.
Tel
001-857-928-2050 or 1-888-588-9418
Fax
001-617-206-9595
Email
sales@chemreagents.com
Country
United States
ProdList
10186
Advantage
62
HBCChem, Inc.
Tel
+1-510-219-6317
Fax
+1-650-486-1361
Email
sales@hbcchem.com
Country
United States
ProdList
10648
Advantage
60
AbaChemScene
Tel
732-484-9848
Fax
888-484-5008
Email
sales@chemscene.com
Country
United States
ProdList
3982
Advantage
60
Alchem Pharmtech,Inc.
Tel
8485655694
Email
sales@alchempharmtech.com
Country
United States
ProdList
63687
Advantage
58
Aladdin Scientific
Tel
+1-+1(833)-552-7181
Email
sales@aladdinsci.com
Country
United States
ProdList
57505
Advantage
58
Aceschem Inc.
Tel
+1-817863-6948 +1-(817)863-6948
Email
sales@aceschem.com
Country
United States
ProdList
19632
Advantage
58
Alfa Chemistry
Tel
--
Fax
--
Email
info@Alfa-Chemistry.com
Country
United States
ProdList
6814
Advantage
0
Thoreau Chem Limited
Tel
--
Fax
--
Email
sales@thoreauchem.com
Country
United States
ProdList
483
Advantage
50
GFS Chemicals Inc
Tel
--
Fax
--
Email
service@gfschemicals.com
Country
United States
ProdList
2329
Advantage
58
SynQuest Laboratories, Inc.
Tel
--
Fax
--
Email
info@synquestlabs.com
Country
United States
ProdList
6871
Advantage
62
Riedel-de Haen AG
Tel
--
Fax
--
Country
United States
ProdList
6773
Advantage
87
TCI America
Tel
--
Fax
--
Email
sales@tciamerica.com
Country
United States
ProdList
6909
Advantage
75
Frontier Scientific, Inc.
Tel
--
Fax
--
Email
sales@frontiersci.com
Country
United States
ProdList
6222
Advantage
86
Matrix Scientific
Tel
--
Fax
--
Email
sales@matrixscientific.com
Country
United States
ProdList
6632
Advantage
80
Morre-Tec Industries, Inc.
Tel
--
Fax
--
Email
sales@morretec.com
Country
United States
ProdList
169
Advantage
64
Allweys LLC
Tel
--
Fax
--
Email
sales@allweysllc.com
Country
United States
ProdList
690
Advantage
30
Anvia Chemicals, LLC
Tel
--
Fax
--
Email
sales@anviachem.com
Country
United States
ProdList
3933
Advantage
0
Louston International
Tel
--
Fax
--
Email
sales@louston.com
Country
United States
ProdList
525
Advantage
58
HBCChem Inc.
Tel
--
Fax
--
Email
sales@hbcchem-inc.com
Country
United States
ProdList
4569
Advantage
30
Rintech, Inc.
Tel
--
Fax
--
Email
info@rintechinc.com
Country
United States
ProdList
3416
Advantage
60
AlliChem, LLC
Tel
--
Fax
--
Email
sales@allichemllc.com
Country
United States
ProdList
6516
Advantage
60
Chem-Impex International, Inc.
Tel
--
Fax
--
Country
United States
ProdList
6730
Advantage
64
ChemService Inc.
Tel
--
Fax
--
Country
United States
ProdList
6379
Advantage
68
Global ChemSources, Inc.
Tel
--
Fax
--
Email
sales@globalchemsources.com
Country
United States
ProdList
132
Advantage
30
Advanced Synthesis Technologies
Tel
--
Fax
--
Email
sales@advancedsynthesis.com
Country
United States
ProdList
4775
Advantage
61
Ryan Scientific, Inc.
Tel
--
Fax
--
Email
ryan.reichlyn@ryansci.com
Country
United States
ProdList
6439
Advantage
60
NetQem
Tel
--
Fax
--
Email
sales@netqem.us
Country
United States
ProdList
1641
Advantage
38
Jubilant Organosys
Tel
--
Fax
--
Email
vamsh@sh163b.sta.net.cn
Country
United States
ProdList
191
Advantage
76
Waterstone Technology, LLC
Tel
--
Fax
--
Email
sales@waterstonetech.com
Country
United States
ProdList
6786
Advantage
30
HONEST JOY HOLDINGS LIMITED
Tel
--
Fax
--
Email
sales@honestjoy.cn
Country
United States
ProdList
6675
Advantage
54
2A PharmaChem USA
Tel
--
Fax
--
Email
sales@2apharmachem.com
Country
United States
ProdList
6137
Advantage
39
3B Scientific Corporation
Tel
--
Fax
--
Email
sales@3bsc.com
Country
United States
ProdList
6718
Advantage
47
Aagile Labs Division of Tyger Scientific
Tel
--
Fax
--
Email
tygersci@yahoo.com
Country
United States
ProdList
6568
Advantage
68
Chemiplus Corporation
Tel
--
Fax
--
Email
okazaki@chemiplus.com
Country
United States
ProdList
3198
Advantage
38
Jubilant Organosys Ltd.
Tel
--
Fax
--
Email
support@jubl.com
Country
United States
ProdList
170
Advantage
81
M/S PANAMIT INTERNATIONAL
Tel
--
Fax
--
Email
sales@jyotichem.com
Country
United States
ProdList
312
Advantage
46
Leonid Chemicals Private Limited
Tel
--
Fax
--
Email
careers@leonidchemicals.com
Country
United States
ProdList
1700
Advantage
43
R. K. Associate
Tel
--
Fax
--
Country
United States
ProdList
194
Advantage
30
Molchemie Overseas
Tel
--
Fax
--
Country
United States
ProdList
59
Advantage
38
Sciencelab.com, Inc.
Tel
--
Fax
--
Email
accounting@sciencelab.com
Country
United States
ProdList
4159
Advantage
82
Advance Scientific & Chemical
Tel
--
Fax
--
Email
sales@advance-scientific.com
Country
United States
ProdList
6419
Advantage
71
Ivy Fine Chemicals
Tel
--
Fax
--
Email
sales@ivychem.com
Country
United States
ProdList
6493
Advantage
58
Alkalimetals
Tel
--
Fax
--
Email
alkalimetals@alkalimetals.com
Country
United States
ProdList
151
Advantage
66
ChemContract Research Inc.
Tel
--
Fax
--
Country
United States
ProdList
1526
Advantage
38
Dishman Europe Ltd
Tel
--
Fax
--
Email
info@dishman-europe.com
Country
United States
ProdList
622
Advantage
58
Chemiceuticals, LLC
Tel
--
Fax
--
Email
sales@chemiceuticals.com
Country
United States
ProdList
1303
Advantage
34
BOSCHE SCIENTIFIC, LLC
Tel
--
Fax
--
Email
Sales@BoscheSci.com
Country
United States
ProdList
6477
Advantage
55
Aagami, Inc.
Tel
--
Fax
--
Email
dinesh@aagami.net
Country
United States
ProdList
557
Advantage
42
American Custom Chemicals Corporation
Tel
--
Fax
--
Email
sales@acccorporation.com
Country
United States
ProdList
6820
Advantage
51
Atlantic SciTech Group, Inc.
Tel
--
Fax
--
Email
sales@astginc.com
Country
United States
ProdList
2308
Advantage
43
More
Less

View Lastest Price from 2-Bromopyridine manufacturers

WUHAN FORTUNA CHEMICAL CO., LTD
Product
2-Bromopyridine 109-04-6
Price
US $0.00-0.00/Kg/Drum
Min. Order
1KG
Purity
99.0%
Supply Ability
10ton/month
Release date
2021-05-28
Hebei Chuanghai Biotechnology Co,.LTD
Product
2-Bromopyridine 109-04-6
Price
US $10.00/KG
Min. Order
1KG
Purity
99.%
Supply Ability
10 ton
Release date
2024-08-21
Wuhan Boyuan Import & Export Co., LTD
Product
2-Bromopyridine 109-04-6
Price
US $6.00/kg
Min. Order
1kg
Purity
99.96%
Supply Ability
500ton
Release date
2023-08-08

109-04-6, 2-BromopyridineRelated Search:


  • Pyridine,2-bromo-
  • 2-BROMOPYRIDINE FOR SYNTHESIS
  • 2-Bromopyridine≥ 99% (GC)
  • 2-BROMOPYRIDINE, 98%2-BROMOPYRIDINE, 98%2-BROMOPYRIDINE, 98%2-BROMOPYRIDINE, 98%
  • TIMTEC-BB SBB003999
  • AKOS BBS-00004324
  • ALPHA-BROMOPYRIDINE
  • BROMOPYRIDINE(2-)
  • 2-BROMO PYRIDINE 2-BROMO PYRIDINE
  • 2-Bromopyridine
  • 2-broMide pyridine
  • 2-BroMopyridine, 99% 100ML
  • 2-BroMopyridine, 99% 25ML
  • 2-bromo-pyridin
  • 2-pyridylbromide
  • beta-bromopyridine
  • -Bromoazine
  • -Bromopyridine
  • o-Bromopyridine
  • 2-Bromopyridine ,99%
  • 2-Brompyridin
  • 2-Bromopyridine &gt
  • 2-Bromopyridine, 99%, for synthesis
  • 2-Bromopyridine,98%
  • 2-Bromopyridine ISO 9001:2015 REACH
  • Orthobromopyridine
  • 109-04-6
  • 105-78-9
  • 109-04-56
  • BrC5H4N
  • C5H4NBr
  • Halopyridines
  • Bromopyridines
  • Pyridines
  • Heterocyclic Building Blocks
  • Halogenated Heterocycles
  • Building Blocks
  • alkyl bromide
  • C5Heterocyclic Building Blocks
  • Halogenated Heterocycles
  • Heterocyclic Building Blocks
  • Bromopyridines
  • Halopyridines
  • Pyridine
  • Pyridines, Pyrimidines, Purines and Pteredines
  • Halides
  • Pyridines
  • Pyridines derivates
  • bc0001
  • 109-04-6