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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)-

Benzonitrile, 4-chloro-3-fluoro-

N#Cc1ccc(c(c1)F)Cl Request for Quotation
Chemical Name: Benzonitrile, 4-chloro-3-fluoro-
CAS Number: 110888-15-8
Product Number: AG0033ZG(AGN-PC-0KK7WA)
Synonyms:
MDL No: MFCD00143291
Molecular Formula: C7H3ClFN
Molecular Weight: 155.5568

Identification/Properties

Properties
MP:
79-81 °C
BP:
214°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
155.556g/mol
XLogP3:
2.4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
154.994g/mol
Monoisotopic Mass:
154.994g/mol
Topological Polar Surface Area:
23.8A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
162
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#:
-
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Chloro-3-fluorobenzonitrile, also known as $name$, serves as a crucial building block in chemical synthesis due to its versatile applications. This compound is extensively utilized in the pharmaceutical industry for the development of novel drugs and active pharmaceutical ingredients (APIs). In organic chemistry, 4-Chloro-3-fluorobenzonitrile acts as a valuable intermediate in the synthesis of various biologically active compounds, such as inhibitors, organic dyes, and agrochemicals. Its unique chemical structure enables it to participate in a wide range of reactions, including nucleophilic substitution, palladium-catalyzed cross-coupling, and heterocyclic chemistry.Moreover, 4-Chloro-3-fluorobenzonitrile plays a crucial role in material science and polymer chemistry. It can be incorporated into polymer structures to modify their physical and chemical properties, leading to the development of new materials with enhanced characteristics.Overall, the versatile nature of 4-Chloro-3-fluorobenzonitrile makes it a valuable asset in chemical synthesis, offering researchers and chemists a wide array of possibilities for creating innovative compounds across various industries.