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ChemicalBook >> CAS DataBase List >>2,4-dibromo-5-methoxyaniline

2,4-dibromo-5-methoxyaniline

CAS No.
35736-52-8
Chemical Name:
2,4-dibromo-5-methoxyaniline
Synonyms
2,4-dibromo-5-methoxyaniline;Benzenamine, 2,4-dibromo-5-methoxy-
CBNumber:
CB32741492
Molecular Formula:
C7H7Br2NO
Molecular Weight:
280.94
MDL Number:
MOL File:
35736-52-8.mol
MSDS File:
SDS
Last updated:2025-08-08 17:45:00
Product description Number Pack Size Price
2,4-Dibromo-5-methoxyaniline KBA73652 5g $295
2,4-Dibromo-5-methoxyaniline 95% AS49480 1g $47
2,4-Dibromo-5-methoxyaniline 95% AS49480 5g $104
2,4-Dibromo-5-methoxyaniline 95% AS49480 25g $323
2,4-Dibromo-5-methoxyaniline 95+% D45868 250mg $44
More product size

2,4-dibromo-5-methoxyaniline Properties

Melting point 136 °C
Boiling point 308.4±37.0 °C(Predicted)
Density 1.897±0.06 g/cm3(Predicted)
storage temp. Keep in dark place,Inert atmosphere,Room temperature
pka 1.41±0.10(Predicted)
Appearance Light green to green Solid

2,4-dibromo-5-methoxyaniline price More Price(30)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Biosynth KBA73652 2,4-Dibromo-5-methoxyaniline 35736-52-8 5g $295 2026-06-04 Buy
Activate Scientific AS49480 2,4-Dibromo-5-methoxyaniline 95% 35736-52-8 1g $47 2026-06-04 Buy
Activate Scientific AS49480 2,4-Dibromo-5-methoxyaniline 95% 35736-52-8 5g $104 2026-06-04 Buy
Activate Scientific AS49480 2,4-Dibromo-5-methoxyaniline 95% 35736-52-8 25g $323 2026-06-04 Buy
Synthonix D45868 2,4-Dibromo-5-methoxyaniline 95+% 35736-52-8 250mg $44 2026-05-06 Buy
Product number Packaging Price Buy
KBA73652 5g $295 Buy
AS49480 1g $47 Buy
AS49480 5g $104 Buy
AS49480 25g $323 Buy
D45868 250mg $44 Buy

2,4-dibromo-5-methoxyaniline Chemical Properties,Uses,Production

Synthesis

m-Anisidine

536-90-3

2-BROMO-5-METHOXYANILINE

59557-92-5

4-BROMO-3-METHOXYANILINE

19056-40-7

2,4-dibromo-5-methoxyaniline

35736-52-8

Using m-aminoanisole (5.00 g, 40.6 mmol) as starting material, it was dissolved in chloroform (40 mL) and the solution was cooled to 5 °C. N-bromosuccinimide (7.23 g, 40.6 mmol) was added to the cooled solution in batches over 1 hour. After addition, the reaction mixture was continued to be stirred in an ice bath at 5-10 °C for 4 hours. Subsequently, the mixture was warmed to room temperature and stirred overnight. Upon completion of the reaction, the reaction mixture was washed sequentially with 2M sodium hydroxide solution (50 mL) and water (60 mL) and then dried over anhydrous sodium sulfate. The solvent was removed by evaporation to give a dark brown viscous liquid. The crude product was separated by silica gel column chromatography (eluent: dichloromethane/hexane, 2:1), first eluting a mixture of 2-bromo-5-methoxyaniline and 2,4-dibromo-5-methoxyaniline. Subsequently, 4-bromo-3-methoxyaniline (860 mg, 10% yield) was eluted as peach-colored crystals with a melting point of 97-98 °C (literature value 93-94 °C); 1H NMR (400 MHz, CDCl3) δ 3.70 (broad single peak, 2H, NH2), 3.80 (single peak, 3H, OCH3), 6.16 (double peaks, J=2.5,8.4 Hz , 1H, ArH), 6.23 (double peaks, J=2.5 Hz, 1H, ArH), 7.23 (double peaks, J=8.4 Hz, 1H, ArH), and the data are in agreement with those reported in the literature. The eluate of the first major band was evaporated to dryness and re-separated by silica gel column chromatography (eluent: ethyl acetate/hexane, 1:2) to afford 2-bromo-5-methoxyaniline (830 mg, 10% yield) as an orange liquid; 1H NMR (400 MHz, CDCl3) δ 3.72 (single peak, 3H, OCH3), 4.07 (broad single peak, 2H NH2), 6.21 (double peak, J=2.9,8.8Hz, 1H, ArH), 6.30 (double peak, J=2.9Hz, 1H, ArH), 7.25 (double peak, J=8.8Hz, 1H, ArH), the data were in agreement with the literature reports. Subsequent elution of the second band gave 2,4-dibromo-5-methoxyaniline (2.66 g, 23% yield) as a brown liquid; Rf (80% ethyl acetate/dichloromethane) 0.87; IR (pure) νmax 3420, 3295, 3176, 2965, 2934, 1620, 1582, 1503, 1278, 1207, 1018 , 805 cm-1; 1H NMR (400 MHz, CDCl3) δ 3.80 (single peak, 3H, OCH3), 4.10 (broad single peak, 2H, NH2), 6.31 (single peak, 1H, ArH), 7.49 (single peak, 1H, ArH); 13C NMR (100 MHz, CDCl3) δ 56.1, 99.3, 99.3 , 99.7, 135.1, 144.3, 155.8; Elemental analysis calculated values (C7H7Br2NO): C 29.93, H 2.51, N 4.99; Measured values: C 30.29, H 2.24, N 4.95%.

References

[1] Journal of Organic Chemistry, 2005, vol. 70, # 7, p. 2870 - 2873
[2] Tetrahedron, 2011, vol. 67, # 32, p. 5798 - 5805

536-90-3
35736-52-8
Synthesis of 2,4-dibromo-5-methoxyaniline from m-Anisidine

2,4-dibromo-5-methoxyaniline Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 36)Suppliers
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View Lastest Price from 2,4-dibromo-5-methoxyaniline manufacturers

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2,4-dibromo-5-methoxyaniline pictures 2022-01-15 2,4-dibromo-5-methoxyaniline
35736-52-8
1KG 98.3% 100 tons Honest Joy Holdings Limited

2,4-dibromo-5-methoxyaniline Spectrum

2,4-dibromo-5-methoxyaniline Benzenamine, 2,4-dibromo-5-methoxy- 35736-52-8
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