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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

Benzene, 2,5-dichloro-1,3-dinitro-

Clc1cc([N+](=O)[O-])c(c(c1)[N+](=O)[O-])Cl Request for Quotation
Chemical Name: Benzene, 2,5-dichloro-1,3-dinitro-
CAS Number: 2213-82-3
Product Number: AG00C4LI(AGN-PC-0JLP6O)
Synonyms:
MDL No:
Molecular Formula: C6H2Cl2N2O4
Molecular Weight: 236.99708

Identification/Properties

Computed Properties
Molecular Weight:
236.992g/mol
XLogP3:
3.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
0
Exact Mass:
235.939g/mol
Monoisotopic Mass:
235.939g/mol
Topological Polar Surface Area:
91.6A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
227
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


2,5-Dichloro-1,3-dinitrobenzene, commonly known as DCNB, is a versatile compound widely used in various chemical synthesis processes. This chemical plays a crucial role in the production of dyes, pharmaceuticals, and agrochemicals due to its unique properties and reactivity.In chemical synthesis, 2,5-Dichloro-1,3-dinitrobenzene is frequently used as a building block for the synthesis of other organic compounds. Its ability to undergo various substitution reactions makes it an essential intermediate in the synthesis of complex molecules. DCNB can be selectively functionalized at different positions, allowing chemists to tailor its structure for specific applications.One of the key applications of 2,5-Dichloro-1,3-dinitrobenzene in chemical synthesis is as a precursor for the synthesis of dyes. By introducing different functional groups to DCNB, chemists can create a wide range of vibrant and colorfast dyes used in textiles, plastics, and other industries. The versatility of DCNB as a dye precursor stems from its ability to undergo diazotization and coupling reactions, leading to a diverse palette of colors.Moreover, 2,5-Dichloro-1,3-dinitrobenzene is also utilized in the pharmaceutical industry for the synthesis of various pharmaceutical compounds. Its presence in the molecular structure of certain drugs imparts specific biological activities, making it a valuable building block in medicinal chemistry. DCNB's role in pharmaceutical synthesis highlights its importance in drug discovery and development processes.Additionally, in agrochemical synthesis, 2,5-Dichloro-1,3-dinitrobenzene serves as a key intermediate for the production of pesticides and herbicides. Its reactivity allows for the creation of potent agricultural chemicals that protect crops from pests and diseases, contributing to global food security.Overall, the application of 2,5-Dichloro-1,3-dinitrobenzene in chemical synthesis spans various industries, showcasing its significance as a versatile and indispensable compound for the creation of diverse organic molecules with tailored properties and functionalities.