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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, 1,4-dichloro-2,5-difluoro-

Fc1cc(Cl)c(cc1Cl)F Request for Quotation
Chemical Name: Benzene, 1,4-dichloro-2,5-difluoro-
CAS Number: 400-05-5
Product Number: AG00CAYS(AGN-PC-0JMOQJ)
Synonyms:
MDL No:
Molecular Formula: C6H2Cl2F2
Molecular Weight: 182.9829

Identification/Properties

Computed Properties
Molecular Weight:
182.979g/mol
XLogP3:
3.4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
181.95g/mol
Monoisotopic Mass:
181.95g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
106
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

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


1,4-Dichloro-2,5-difluorobenzene, is a versatile compound widely used in chemical synthesis. It serves as a valuable building block in the creation of various organic compounds and materials. This compound is particularly useful in the pharmaceutical industry, where it is employed in the synthesis of pharmaceutical intermediates and active ingredients. Its unique molecular structure enables it to participate in various reactions, such as halogenation, arylation, and nucleophilic substitution, making it a crucial component in the production of complex molecules. Additionally, 1,4-Dichloro-2,5-difluorobenzene finds application in the manufacturing of agrochemicals, functional materials, and specialty chemicals, highlighting its significance in modern chemistry.