| Identification | Back Directory | [Name]
2,4-Dibromonitrobenzene | [CAS]
51686-78-3 | [Synonyms]
4-Dibromonitrobenzene
2,4-Dibromonitrobenzene
,3-Dibromo-4-nitrobenzene
1,3-Dibromo-4-nitrobenzene
2,4-Dibromo-1-nitrobenzene
Benzene, 2,4-dibroMo-1-nitro-
2,4-Dibromo-1-nitrobenzene>
1,3-Dibromo-4-nitrobenzene,98%
2,4-Dibromonitrobenzene 51686-78-3 | [Molecular Formula]
C6H3Br2NO2 | [MDL Number]
MFCD02660416 | [MOL File]
51686-78-3.mol | [Molecular Weight]
280.902 |
| Chemical Properties | Back Directory | [Melting point ]
61-62℃ | [Boiling point ]
270℃ | [density ]
2.101 | [refractive index ]
1.6400 (estimate) | [Fp ]
117℃ | [storage temp. ]
Sealed in dry,Room Temperature | [solubility ]
soluble in Methanol | [form ]
Crystalline Powder | [color ]
Yellow | [InChI]
InChI=1S/C6H3Br2NO2/c7-4-1-2-6(9(10)11)5(8)3-4/h1-3H | [InChIKey]
DXRVYZGVVFZCFP-UHFFFAOYSA-N | [SMILES]
C1([N+]([O-])=O)=CC=C(Br)C=C1Br |
| Hazard Information | Back Directory | [Description]
2,4-Dibromo-1-nitrobenzene is a pharmaceutical intermediate that can be obtained by nitration of m-dibromobenzene. This compound can be used to prepare the benzimidazole anthelmintic fenbendazole through a four-step reaction. | [Chemical Properties]
Light yellow powder | [Uses]
2,4-Dibromo-1-nitrobenzene is used as pharmaceutical and pesticide intermediates. | [Production Methods]
Dissolve 24.5g of m-dibromobenzene in 49.0g of concentrated sulfuric acid (98%) at room temperature, cool to 0-5°C, add 9.80g of nitric acid (68%) dropwise, control the temperature at 0-5°C during the addition process, and stir at 5-10°C for 2 hours after the addition is complete. After the reaction is completed, add the reaction solution dropwise to 49.0g of cold water, and the temperature does not exceed 60°C during the quenching process. After the quenching is completed, stir at room temperature for 0.5 hours, filter, and wash the filter cake with 15.0g of water to obtain 31.95g (water content 16.0%) of 2,4-Dibromo-1-nitrobenzene tide product with a purity of 99.75%. | [References]
[1] European Journal of Medicinal Chemistry, 2017, vol. 126, p. 590 - 603
[2] Patent: WO2004/14900, 2004, A1. Location in patent: Page 24; 57-58
[3] Journal of Organic Chemistry, 2011, vol. 76, # 19, p. 8088 - 8094
[4] Heteroatom Chemistry, 2009, vol. 20, # 2, p. 101 - 108
[5] Physical Chemistry Chemical Physics, 2018, vol. 20, # 25, p. 17504 - 17516 |
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Alfa Aesar
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