ChemicalBook > CAS DataBase List > 2,5-Dibromopyridine

2,5-Dibromopyridine

Product Name
2,5-Dibromopyridine
CAS No.
624-28-2
Chemical Name
2,5-Dibromopyridine
Synonyms
Dibromopyridine;NSC 76597;5-DibroMopyridine;2,5-Dibrompyridin;2,5-dibromopyridin;2,5 dibromopyrdine;2,5-DIBROMOPYRIDINE;3,6-DibroMopyridine;2,5 Di bromo pyridne;Perampanel Impurity 9
CBNumber
CB7283491
Molecular Formula
C5H3Br2N
Formula Weight
236.89
MOL File
624-28-2.mol
More
Less

2,5-Dibromopyridine Property

Melting point:
92-95 °C (lit.)
Boiling point:
235 °C / 772mmHg
Density 
2.0383 (rough estimate)
refractive index 
1.5800 (estimate)
Flash point:
62℃
storage temp. 
Inert atmosphere,Room Temperature
solubility 
Chloroform (Slightly), Methanol (Slightly)
pka
-1.57±0.10(Predicted)
form 
Crystalline Powder
color 
Almost white or light beige to brown
Water Solubility 
insoluble
BRN 
109099
InChI
InChI=1S/C5H3Br2N/c6-4-1-2-5(7)8-3-4/h1-3H
InChIKey
ZHXUWDPHUQHFOV-UHFFFAOYSA-N
SMILES
C1(Br)=NC=C(Br)C=C1
CAS DataBase Reference
624-28-2(CAS DataBase Reference)
More
Less

Safety

Hazard Codes 
Xi,Xn
Risk Statements 
36/37/38-20/21/22
Safety Statements 
26-37/39-36/37/39-36
RIDADR 
UN2811
WGK Germany 
3
HazardClass 
IRRITANT
HS Code 
29333999
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P270Do not eat, drink or smoke when using this product.

P271Use only outdoors or in a well-ventilated area.

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

P304+P340IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing.

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

P405Store locked up.

P501Dispose of contents/container to..…

More
Less

N-Bromosuccinimide Price

Sigma-Aldrich
Product number
D43107
Product name
2,5-Dibromopyridine
Purity
98%
Packaging
10g
Price
$96.9
Updated
2024/03/01
TCI Chemical
Product number
D1217
Product name
2,5-Dibromopyridine
Purity
>99.0%(GC)
Packaging
5g
Price
$24
Updated
2024/03/01
TCI Chemical
Product number
D1217
Product name
2,5-Dibromopyridine
Purity
>99.0%(GC)
Packaging
25g
Price
$66
Updated
2024/03/01
Alfa Aesar
Product number
A10937
Product name
2,5-Dibromopyridine, 97%
Packaging
10g
Price
$70.65
Updated
2024/03/01
Alfa Aesar
Product number
A10937
Product name
2,5-Dibromopyridine, 97%
Packaging
50g
Price
$257.65
Updated
2024/03/01
More
Less

2,5-Dibromopyridine Chemical Properties,Usage,Production

Description

Pyridine and its derivatives are distributed widely by nature. Many plant constituents are as contain pyridine ring compounds in the structure of alkaloids, etc.; they are the bases producing many vital compounds and are indispensable raw materials during medicine, agricultural chemicals, dyestuff, tension-active agents, rubber ingredients, fodder additives, foodstuff additives, tackiness agents, etc. are produced.2,5-dibromo pyridine is an important intermediate of organic synthesis and is mainly used in medicine intermediate, organic synthesis, and organic solvent, can also be applicable to aspects such as DYE PRODUCTION, pesticide production and spices. Selective monolithiation of 2,5-dibromopyridine at either the 2-position or the 5-position is reported. Solvent and concentration strongly influence the selectivity. Coordinating solvents and higher concentration favour the 5-position, while non-coordinating solvents and lower concentration favour the 2-position[1].

Chemical Properties

2,5-Dibromopyridine is an off-white crystalline solid. It is insoluble in water but soluble in strong polar organic solvents. It exhibits strong alkalinity.

Uses

2,5-Dibromopyridine (cas# 624-28-2) is a compound useful in organic synthesis.

Preparation

To synthesize 2,5-dibromopyridine, follow these steps:
Add 2-amino-5-bromopyridine (13.0 kg) into a water-cooled solution at 10 °C.
Slowly add 47% aqueous hydrogen bromide (37 L) to the mixture.
Introduce liquid bromine (11 L) into the mixture.
Maintain the reaction temperature below 10 °C.
Prepare a solution of NaNO2 (16.1 kg) and H2O (19 L) and add it dropwise to the mixture while keeping the temperature between 0-5 °C.
Stir the reaction mixture for 30 minutes.
Treat the mixture with a solution of NaOH (28.0 kg) in water (30 L) at a controlled rate below 20-25 °C.
Extract the reaction mixture with diethyl ether (3 × 40 L).
Dry the organic layer with anhydrous Na2SO4.
Remove the desiccant by filtration.
Evaporate the resulting filtrate under reduced pressure to dryness.
Suspend the residue in heptane (10 L).
Collect the target product molecule, 2,5-dibromopyridine, by filtration.
Synthesis method of 2,5-dibromopyridine

References

[1] Xin Wang. “Selective monolithiation of 2,5-dibromopyridine with butyllithium.” Tetrahedron Letters 41 1 (2000): 4335–4338.

More
Less

2,5-Dibromopyridine Suppliers

Carbosynth
Tel
--
Fax
--
Email
sales@carbosynth.com
Country
United Kingdom
ProdList
6005
Advantage
58
Biokemix
Tel
--
Fax
--
Email
info@biokemix.com
Country
United Kingdom
ProdList
1066
Advantage
58
Melrob Ltd (part of Nordmann)
Tel
--
Fax
--
Email
nquiries@melrob.com
Country
United Kingdom
ProdList
3065
Advantage
58
Fisher Scientific Uk Ltd.
Tel
--
Fax
--
Email
.international@thermofisher.com
Country
United Kingdom
ProdList
2932
Advantage
58
Molekula Limited
Tel
--
Fax
--
Email
o@molekula.com
Country
United Kingdom
ProdList
6127
Advantage
58
Apollo Scientific Ltd
Tel
--
Fax
--
Email
ales@apo
Country
United Kingdom
ProdList
4521
Advantage
58
NiCHe Materials Ltd.
Tel
--
Fax
--
Email
Mike.Norman@NiCHeMaterials.com
Country
United Kingdom
ProdList
891
Advantage
58
Maybridge Chemical Co. Ltd.
Tel
--
Fax
--
Email
maybridge.sales@thermofisher.com
Country
United Kingdom
ProdList
277
Advantage
58
Biosynth Carbosynth
Tel
--
Fax
--
Email
ales@carbosynth.com
Country
United Kingdom
ProdList
2598
Advantage
58
Manchester Organics
Tel
--
Fax
--
Email
info@manchesterorganics.com
Country
United Kingdom
ProdList
6834
Advantage
67
Apollo Scientific Ltd.
Tel
--
Fax
--
Email
sales@apolloscientific.co.uk
Country
United Kingdom
ProdList
6084
Advantage
88
Molekula Ltd
Tel
--
Fax
--
Email
info@molekula.com
Country
United Kingdom
ProdList
4060
Advantage
50
Carbosynth Limited
Tel
--
Fax
--
Email
sales@carbosynth.com
Country
United Kingdom
ProdList
6581
Advantage
61
Leancare Ltd.
Tel
--
Fax
--
Email
enquiry@leancare.co.uk
Country
United Kingdom
ProdList
6446
Advantage
42
CARBONE SCIENTIFIC CO.,LTD
Tel
--
Fax
--
Email
sales@carbonesci.com
Country
United Kingdom
ProdList
6666
Advantage
30
Hawks Scientific Ltd
Tel
--
Fax
--
Email
pete@hawks-scientific.com
Country
United Kingdom
ProdList
2221
Advantage
43
Apin Chemicals Limited (UK)
Tel
--
Fax
--
Email
info@apinchemicals.com
Country
United Kingdom
ProdList
6184
Advantage
60
Atlantic Research Chemicals Ltd.
Tel
--
Fax
--
Email
info@atlantic-chemicals.com
Country
United Kingdom
ProdList
5618
Advantage
63
CMS Chemicals Limited
Tel
--
Fax
--
Email
cms.marketing@cms-chemicals.com
Country
United Kingdom
ProdList
3708
Advantage
60
MOLEKULA Ltd.
Tel
--
Fax
--
Email
kevinbanks@molekula.com
Country
United Kingdom
ProdList
6140
Advantage
66
ETA SCIENTIFIC Co.,Ltd
Tel
--
Fax
--
Email
sales@etascientific.com
Country
United Kingdom
ProdList
6090
Advantage
34
UK GREEN SCIENTIFIC CO.,LIMITED
Tel
--
Fax
--
Email
sales@gs-chem.com
Country
United Kingdom
ProdList
6098
Advantage
47
Fluorochem Ltd
Tel
--
Fax
--
Email
vernam@fluorochem.co.uk
Country
United Kingdom
ProdList
6375
Advantage
65
Fluorochem Ltd.
Tel
--
Fax
--
Email
enquiries@fluorochem.co.uk
Country
United Kingdom
ProdList
6401
Advantage
74
Apin Chemicals Ltd.
Tel
--
Fax
--
Email
info@apinchemicals.com
Country
United Kingdom
ProdList
6807
Advantage
42
VWR International
Tel
--
Fax
--
Email
solutions@vwr.com
Country
United Kingdom
ProdList
6548
Advantage
82
Gee Lawson Ltd.
Tel
--
Fax
--
Email
chemical@geelawson.co.uk
Country
United Kingdom
ProdList
70
Advantage
65
Fulcrum Scientific Ltd.
Tel
--
Fax
--
Country
United Kingdom
ProdList
6565
Advantage
38
Eurolabs Limited
Tel
--
Fax
--
Country
United Kingdom
ProdList
6309
Advantage
46
More
Less

View Lastest Price from 2,5-Dibromopyridine manufacturers

Hebei Mujin Biotechnology Co.,Ltd
Product
2,5-Dibromopyridine 624-28-2
Price
US $0.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
50000KG/month
Release date
2023-09-12
Watson Biotechnology Co.,Ltd
Product
2,5-Dibromopyridine 624-28-2
Price
US $0.00-0.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
20MT
Release date
2024-08-02
Shanghai UCHEM Inc.
Product
2,5-Dibromopyridine 624-28-2
Price
US $136.00/kg
Min. Order
1kg
Purity
0.99
Supply Ability
100kg
Release date
2023-11-17

624-28-2, 2,5-DibromopyridineRelated Search:


  • 2,5-DIBROMOPYRIDINE
  • PYRIDINE, 2,5-DIBROMO-
  • Dibromopyridine
  • 2,5-Dibromopyridine, 97+%
  • 2,5-dibromopyridin
  • 2,5-DIBROMOPYRIDINE 2,5-DIBROMOPYRIDINE
  • 2,5-Dibromo pyridine ,98%
  • 2,5-DibroMopyridine, 97% 10GR
  • 3,6-DibroMopyridine
  • NSC 76597
  • 5-DibroMopyridine
  • 2, 5-2 broMide pyridine
  • 2,5 Di bromo pyridne
  • 2,5-Dibromopyridine &gt
  • Perampanel Impurity 9
  • 2,5-Dibromopyridine ISO 9001:2015 REACH
  • 2,5-Dibrompyridin
  • 2,5 dibromopyrdine
  • Hot Sale?2, 5-Dibromopyridine CAS?624-28-2?with Best Price
  • Pyronoprene Impurity 17
  • Nicotinic Acid Impurity 13
  • 624-28-2
  • 324-28-2
  • Building Blocks
  • Pyridines
  • Halogenated Heterocycles
  • Heterocyclic Building Blocks
  • Bromopyridines
  • Halopyridines
  • alkyl bromide
  • Building Blocks
  • C5
  • Chemical Synthesis
  • Halogenated Heterocycles
  • Heterocyclic Building Blocks
  • Brominated heterocyclic series
  • Aromatics
  • Bases & Related Reagents
  • Nucleotides
  • Aromatics Compounds
  • Bromopyridines
  • Halopyridines
  • Pyridine series
  • C5Heterocyclic Building Blocks
  • Halogenated Heterocycles
  • Heterocyclic Building Blocks
  • Nitrogen cyclic compounds
  • blocks
  • Bromides
  • Pyridines
  • pyridine derivative
  • Pyridines, Pyrimidines, Purines and Pteredines
  • Halides
  • Pyridine
  • Pyridines derivates
  • bc0001
  • 624-28-2