Description

2,4-Dibromoaniline (CAS No. 615-57-6) is a high-purity halogenated aniline derivative with the molecular formula C₆H₅Br₂N. This aromatic amine features two bromine atoms at the 2- and 4-positions of the aniline ring, offering unique reactivity for electrophilic substitution and coupling reactions. Ideal for pharmaceutical intermediates, agrochemical synthesis, and advanced material research, our product is rigorously tested to ensure ≥98% purity (HPLC) with minimal trace impurities. Supplied as a light yellow to beige crystalline powder, it is packaged under inert conditions to ensure stability. Suitable for use in Suzuki-Miyaura cross-coupling, Buchwald-Hartwig amination, and other palladium-catalyzed transformations. Store in a cool, dry place away from light and oxidizing agents.

Properties

• CAS Number: 615-57-6
• Complexity: 97.1
• IUPAC Name: 2,4-dibromoaniline
• InChI: InChI=1S/C6H5Br2N/c7-4-1-2-6(9)5(8)3-4/h1-3H,9H2
• InChI Key: DYSRXWYRUJCNFI-UHFFFAOYSA-N
• Exact Mass: 250.87682
• Molecular Formula: C6H5Br2N
• Molecular Weight: 250.92
• SMILES: C1=CC(=C(C=C1Br)Br)N
• Topological: 26
• Monoisotopic Mass: 248.87887
• Synonyms: 2,4-DIBROMOANILINE, 615-57-6, Benzenamine, 2,4-dibromo-, 2,4-dibromobenzenamine, NSC 88324, 8D6YF8BB75, ANILINE, 2,4-DIBROMO-, EINECS 210-434-4, NSC-88324, DTXSID4060654, DTXCID9043063, 210-434-4, inchi=1/c6h5br2n/c7-4-1-2-6(9)5(8)3-4/h1-3h,9h, 2.4-Dibromoaniline, MLS000737163, 63505-64-6, 2,4-Dibromo-phenylamine, Dibromobenzenamine, 2,4-Dibromanilin, NSC88324, MFCD00007633, 2,4-dibromophenylamine, 2,4-di-bromo-aniline, Benzenamine,4-dibromo-, 2,4-bis(bromanyl)aniline, NCIOpen2_005148, UNII-8D6YF8BB75, 2,4-Dibromoaniline, 98%, SCHEMBL417742, SCHEMBL2039309, SCHEMBL3173111, SCHEMBL7053961, SCHEMBL9760330, CHEMBL1710125, HMS2884A04, STR01937, STL497388, AKOS000113480, NCGC00246894-01, AC-17039, SMR000528396, DB-024168, D1153, NS00005239, ST50406290, EN300-20283, A833299, Z104477574

Application

2,4-Dibromoaniline serves as a versatile building block in organic synthesis, particularly in the preparation of brominated heterocycles and active pharmaceutical ingredients (APIs). It is widely employed in palladium-catalyzed cross-coupling reactions to construct biaryl scaffolds for drug discovery. Additionally, this compound finds use in agrochemical research as a precursor for herbicides and fungicides. Its bromine substituents enable further functionalization via halogen-metal exchange or nucleophilic aromatic substitution.

Safety and Hazards

GHS Hazard Statements

• H301 (89.4%): Toxic if swallowed [Danger Acute toxicity, oral]
• H302 (10.6%): Harmful if swallowed [Warning Acute toxicity, oral]
• H315 (97.9%): Causes skin irritation [Warning Skin corrosion/irritation]
• H319 (97.9%): Causes serious eye irritation [Warning Serious eye damage/eye irritation]
• H332 (10.6%): Harmful if inhaled [Warning Acute toxicity, inhalation]
• H335 (95.7%): May cause respiratory irritation [Warning Specific target organ toxicity, single exposure; Respiratory tract irritation]

Precautionary Statements

• P261, P264, P264+P265, P270, P271, P280, P301+P316, P301+P317, P302+P352, P304+P340, P305+P351+P338, P317, P319, P321, P330, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501

Hazard Classes and Categories

• Acute Tox. 3 (89.4%)
• Acute Tox. 4 (10.6%)
• Skin Irrit. 2 (97.9%)
• Eye Irrit. 2 (97.9%)
• Acute Tox. 4 (10.6%)
• STOT SE 3 (95.7%)

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Disclaimer: Sold exclusively for laboratory research. Prohibited for commercial use, diagnostics, or human/animal applications. Buyers assume all compliance liability.