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2,3-Dibromo-5-methylpyridine

CAS No.
29232-39-1
Chemical Name:
2,3-Dibromo-5-methylpyridine
Synonyms
2,3-DIBROMO-5-METHYL;5,6-Dibromo-3-picoline;5,6-Dibromo-m-picoline;2,3-DIBROMO-5-PICOLINE;2,3-Dibromo-5-methylpyridine;Pyridine,2,3-dibroMo-5-Methyl-;2,3-DIBROMO-5-METHYLPYRIDINE 98%;3-Bromo-6-hydroxy-3-methylpyridine;5,6-dibromo-3-methyl-3,4-dihydropyridine;2,3-DIBROMO-5-METHYLPYRIDINE ISO 9001:2015 REACH
CBNumber:
CB9415294
Molecular Formula:
C6H5Br2N
Molecular Weight:
250.92
MDL Number:
MFCD04112574
MOL File:
29232-39-1.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-09-12 18:56:28

2,3-Dibromo-5-methylpyridine Properties

Melting point 53.0 to 57.0 °C
Boiling point 270.8±35.0 °C(Predicted)
Density 1.911±0.06 g/cm3(Predicted)
Flash point >110℃
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
solubility soluble in Methanol
pka -1.27±0.20(Predicted)
form powder to crystal
color White to Light yellow to Light orange
InChI 1S/C6H5Br2N/c1-4-2-5(7)6(8)9-3-4/h2-3H,1H3
InChIKey BZUZAZMAGVFIBS-UHFFFAOYSA-N
SMILES Cc1cnc(Br)c(Br)c1
CAS DataBase Reference 29232-39-1(CAS DataBase Reference)
UNSPSC Code 12352100

SAFETY

Risk and Safety Statements

Symbol(GHS)  Corrosion (GHS05)Skull and Crossbones (GHS06)
GHS05,GHS06
Signal word  Danger
Hazard statements  H301-H318
Precautionary statements  P280-P301+P310+P330-P305+P351+P338+P310
Hazard Codes  Xi,T
Risk Statements  20/21/22-36/37/38-41-25
Safety Statements  26-36/37/39-45-39
RIDADR  UN 2811 6.1 / PGIII
WGK Germany  3
HazardClass  IRRITANT
HS Code  2933399990
Storage Class 6.1C - Combustible acute toxic Cat.3
toxic compounds or compounds which causing chronic effects
Hazard Classifications Acute Tox. 3 Oral
Eye Dam. 1
NFPA 704
1
3 0

2,3-Dibromo-5-methylpyridine price More Price(60)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 715727 2,3-Dibromo-5-methylpyridine 97% 29232-39-1 1g $50.5 2023-01-07 Buy
TCI Chemical D5100 2,3-Dibromo-5-methylpyridine >98.0%(GC) 29232-39-1 5g $45 2026-04-30 Buy
TCI Chemical D5100 2,3-Dibromo-5-methylpyridine >98.0%(GC) 29232-39-1 25g $228 2021-12-16 Buy
Usbiological 273466 2,3-Dibromo-5-methylpyridine Asreported 29232-39-1 1g $319 2026-06-03 Buy
Usbiological 273466 2,3-Dibromo-5-methylpyridine Asreported 29232-39-1 2g $429 2026-06-03 Buy
Product number Packaging Price Buy
715727 1g $50.5 Buy
D5100 5g $45 Buy
D5100 25g $228 Buy
273466 1g $319 Buy
273466 2g $429 Buy

2,3-Dibromo-5-methylpyridine Chemical Properties, Uses, Production

Uses

2,3-Dibromo-5-methylpyridine serves as a substrate for the synthesis of heterocyclic phenothiazines and regioselective cross-coupling products[2][3]. It functions as an additive in iododesilylation reactions, where it provides a slight yield improvement compared to other pyridine-based additives[1].

Synthesis

2-Amino-3-bromo-5-methylpyridine

17282-00-7

2,3-DIBROMO-5-METHYLPYRIDINE

29232-39-1

2-Amino-3-bromo-5-methylpyridine (187 mg, 1.00 mmol) was added to a 30 mL three-necked flask, followed by the addition of 48% aqueous hydrogen bromide (1 mL) to dissolve the feedstock. The reaction mixture was cooled in an ice bath, keeping the internal temperature in the range of 2 to 5 °C, and bromine (154 μL, 3.00 mmol) was slowly added dropwise. After the dropwise addition, stirring was continued at the same temperature for 10 min. Subsequently, a solution of sodium nitrite (174 mg, 2.5 mmol) dissolved in water (500 μL) was added dropwise to the reaction system while keeping the temperature unchanged, and stirring was continued for 1 h after completion of the dropwise addition. After completion of the reaction, a solution of sodium hydroxide (377 mg, 9.4 mmol) dissolved in water (2 mL) was added slowly and the mixture was stirred for 1 h at room temperature. The reaction solution was transferred to a partition funnel and separated by extraction with ethyl acetate (10 mL) and water (10 mL), and the aqueous phase was extracted once more with ethyl acetate (10 mL). The organic phases were combined and washed sequentially with 5% aqueous sodium sulfite (5 mL) and saturated saline (10 mL), then dried with anhydrous sodium sulfate. The solvent was removed by distillation under reduced pressure to afford the target product 2,3-dibromo-5-methylpyridine (244 mg, 0.97 mmol) as a yellow solid in 97% yield. The product was analyzed by 1H-NMR (CDCl3, TMS, 300 MHz) δ (ppm): 2.30 (s, 3H), 7.73 (d, 1H, J = 1.5 Hz), 8.14 (d, 1H, J = 1.2 Hz); 13C-NMR (CDCl3, TMS, 300 MHz) δ (ppm): 17.41, 123.16. 134.13, 140.39, 142.29, 148.57; high-resolution mass spectrometry (C6H5Br2N) Theoretical: [M+] 248.8789, Measured: [M+] 248.8786; Melting point 54.2 °C.

References

[1]Bloux, H., Dahiya, A., Hébert, A., Fabis, F., Schoenebeck, F., & Cailly, T. (2023). Base‐Mediated Radio‐Iodination of Arenes by Using Organosilane and Organogermane as Radiolabelling Precursors. Chemistry – A European Journal, 29(19). https://doi.org/10.1002/chem.202203366
[2]Hu, W., & Zhang, S. (2015). Method for the Synthesis of Phenothiazines via a Domino Iron-Catalyzed C–S/C–N Cross-Coupling Reaction. The Journal of Organic Chemistry, 80(12), 6128–6132. https://doi.org/10.1021/acs.joc.5b00568
[3]Hikawa, H., &amp; Yokoyama, Y. (2010). Cross-coupling reaction on N-(3,5-dibromo-2-pyridyl)piperazines: regioselective synthesis of 3,5-disubstituted pyridylpiperazines. <i>Tetrahedron</i>, <i>66 49</i>, Pages 9552-9559. https://doi.org/10.1016/j.tet.2010.09.100

17282-00-7
29232-39-1
Synthesis of 2,3-Dibromo-5-methylpyridine from 2-Amino-3-bromo-5-methylpyridine

2,3-Dibromo-5-methylpyridine Preparation Products And Raw materials

Global Suppliers ( 226)
Supplier Tel Email Country ProdList Advantage
J & K SCIENTIFIC LTD. 18210857532 18210857532 jkinfo@jkchemical.com China 96815 76
Meryer (Shanghai) Chemical Technology Co., Ltd. 4006356688 18621169109 market03@meryer.com China 40202 62
Liaoning Tianhua Chemical Co., Ltd. 0418-6530555 2855550 China 338 69
Alfa Aesar 400-6106006 saleschina@alfa-asia.com China 30103 84
ShangHai DEMO Chemical Co.,Ltd 400-021-7337 2355568890 sales@demochem.com China 2569 57
Energy Chemical 400-0056266 sales8178@energy-chemical.com China 44850 61
Wuhan Chemwish Technology Co., Ltd 86-027-67849912 sales@chemwish.com China 35884 56
Capot Chemical Co., Ltd +86 (0) 571 85 58 67 18 China 18187 66
Beijing Ouhe Technology Co., Ltd 13552068683 13522913783 2355560935@qq.com China 11777 60
JinYan Chemicals(ShangHai) Co.,Ltd. 13817811078 sales@jingyan-chemical.com China 9963 60

View Latest Price from 2,3-Dibromo-5-methylpyridine manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
2,3-Dibromo-5-picoline pictures 2026-09-02 2,3-Dibromo-5-picoline
29232-39-1
$1.00-200.00 1KG 99%, 99.5% Sublimated Henan Fengda Chemical Co., Ltd
2,3-DIBROMO-5-METHYLPYRIDINE  pictures 2026-08-20 2,3-DIBROMO-5-METHYLPYRIDINE
29232-39-1
$1.10 1g 99.00% 100 Tons Min Dideu Industries Group Limited
2,3-DIBROMO-5-METHYLPYRIDINE pictures 2026-06-30 2,3-DIBROMO-5-METHYLPYRIDINE
29232-39-1
1KG 98.0% 10000KGS Shaanxi Dideu New Materials Co. Ltd

2,3-Dibromo-5-methylpyridine Spectrum

Pyridine,2,3-dibroMo-5-Methyl- 2,3-DIBROMO-5-PICOLINE 2,3-DIBROMO-5-METHYLPYRIDINE 98% 2,3-DIBROMO-5-METHYL 5,6-Dibromo-m-picoline 5,6-Dibromo-3-picoline 5,6-dibromo-3-methyl-3,4-dihydropyridine 3-Bromo-6-hydroxy-3-methylpyridine 2,3-DIBROMO-5-METHYLPYRIDINE ISO 9001:2015 REACH 2,3-Dibromo-5-methylpyridine 29232-39-1 Heterocycle-Pyridine series pyridine series Pyridines Variety of halogenated heterocyclic series Pyridine