Description
2,5-Dichloro-1,3-dinitrobenzene (CAS No. 2213-82-3) is a high-purity aromatic compound with the molecular formula C6H2Cl2N2O4, widely utilized in organic synthesis and specialty chemical applications. This yellow crystalline solid exhibits excellent stability and reactivity, making it a valuable intermediate for pharmaceuticals, agrochemicals, and dyestuff production. Its IUPAC name, 2,5-dichloro-1,3-dinitrobenzene, reflects its precise structural configuration, featuring two chlorine and two nitro functional groups on a benzene ring. Our product is rigorously tested for purity (>98%) via HPLC/GC analysis, ensuring optimal performance in nucleophilic substitution reactions and electrophilic aromatic substitutions. Packaged under inert conditions to prevent degradation, it is available in research (1g-100g) and bulk (1kg+) quantities with customizable purity grades.
Properties
- CAS Number: 2213-82-3
- Complexity: 227
- IUPAC Name: 2,5-dichloro-1,3-dinitro-benzene
- InChI: InChI=1S/C6H2Cl2N2O4/c7-3-1-4(9(11)12)6(8)5(2-3)10(13)14/h1-2H
- InChI Key: AGGUKALRPKAKSM-UHFFFAOYSA-N
- Exact Mass: 235.9391619
- Molecular Formula: C6H2Cl2N2O4
- Molecular Weight: 236.99
- SMILES: C1=C(C=C(C(=C1[N+](=O)[O-])Cl)[N+](=O)[O-])Cl
- Topological: 91.6
- Monoisotopic Mass: 235.9391619
- Synonyms: 2,5-Dichloro-1,3-dinitrobenzene, 2213-82-3, 1,4-Dichloro-2,6-dinitrobenzene, 2,6-Dinitro-1,4-dichlorobenzene, UNII-32VX4DFV3R, 32VX4DFV3R, Benzene, 2,5-dichloro-1,3-dinitro-, EINECS 218-673-6, NSC 67758, NSC-67758, DTXSID6062256, DTXCID7036614, 218-673-6, 2,?5-?Dichloro-?1,?3-?Dinitrobenzene, NSC67758, 2,3-dinitrobenzene, SCHEMBL9452603, AGGUKALRPKAKSM-UHFFFAOYSA-N, Benzene,5-dichloro-1,3-dinitro-, 2,5-dichloro-1,3-dinitro-benzene, MFCD00068222, SY351139, NS00027075, A1-02815, Q27256195
Application
2,5-Dichloro-1,3-dinitrobenzene serves as a key precursor in the synthesis of herbicides and fungicides due to its electrophilic aromatic substitution reactivity. It is employed in pharmaceutical research for constructing heterocyclic scaffolds via nitro-group reduction and subsequent cyclization. The compound also finds use in dye manufacturing as an intermediate for azo and sulfur dyes. Its dichloro-dinitro structure enables selective functionalization in cross-coupling reactions for advanced material science applications.
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