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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)-

1,3-dichloro-2-fluoro-5-iodobenzene

Ic1cc(Cl)c(c(c1)Cl)F Request for Quotation
Chemical Name: 1,3-dichloro-2-fluoro-5-iodobenzene
CAS Number: 133307-08-1
Product Number: AG0014LK(AGN-PC-02KKM2)
Synonyms:
MDL No:
Molecular Formula: C6H2Cl2FI
Molecular Weight: 290.8890

Identification/Properties

Computed Properties
Molecular Weight:
290.885g/mol
XLogP3:
3.9
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
289.856g/mol
Monoisotopic Mass:
289.856g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
110
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


5-Iodo-1,3-dichloro-2-fluorobenzene is a versatile compound commonly used in chemical synthesis for numerous applications due to its unique properties. This compound can serve as a valuable building block in the creation of various pharmaceuticals, agrochemicals, and advanced materials. Its precise structure allows for selective functionalization, making it an important intermediate in the synthesis of complex organic molecules. Additionally, 5-Iodo-1,3-dichloro-2-fluorobenzene can participate in cross-coupling reactions, providing a pathway for the formation of carbon-carbon and carbon-heteroatom bonds. Its presence in the synthesis process can enhance the efficiency and specificity of reactions, leading to improved yields and purity in the final product. In conclusion, the application of 5-Iodo-1,3-dichloro-2-fluorobenzene in chemical synthesis offers a vital contribution to the development of diverse compounds with significant industrial and scientific importance.