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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)-

3-fluoro-5-iodophenol

Oc1cc(F)cc(c1)I Request for Quotation
Chemical Name: 3-fluoro-5-iodophenol
CAS Number: 939771-60-5
Product Number: AG00H329(AGN-PC-0H2X3V)
Synonyms:
MDL No:
Molecular Formula: C6H4FIO
Molecular Weight: 237.9982332

Identification/Properties

Computed Properties
Molecular Weight:
238g/mol
XLogP3:
2.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
237.92909g/mol
Monoisotopic Mass:
237.92909g/mol
Topological Polar Surface Area:
20.2Ų
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
99.1
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


3-Fluoro-5-iodophenol, also known as $name$, is a versatile chemical compound widely utilized in modern chemical synthesis processes. With its unique molecular structure, this compound plays a crucial role in various organic reactions and transformations. One of the primary applications of 3-Fluoro-5-iodophenol is in the field of pharmaceuticals. As a key building block, it serves as a valuable precursor in the synthesis of biologically active compounds and pharmaceutical intermediates. Its incorporation into drug molecules can significantly enhance their pharmacological properties and therapeutic effects.In addition, 3-Fluoro-5-iodophenol is commonly used in the production of agrochemicals and specialty chemicals. By undergoing different chemical reactions, it can be transformed into complex structures that exhibit specific pesticidal or herbicidal activities. This compound's versatility makes it a valuable tool for designing novel agricultural products with improved efficacy and environmental safety.Furthermore, 3-Fluoro-5-iodophenol is employed in academic research and material science applications. Its ability to undergo diverse chemical transformations allows researchers to explore new reaction pathways and develop innovative materials with unique properties. From catalyst design to material synthesis, this compound contributes to advancements in various scientific disciplines.Overall, 3-Fluoro-5-iodophenol's role in chemical synthesis extends beyond traditional boundaries, offering a wide range of possibilities for creating valuable products and advancing scientific knowledge.