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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)-

2-(2-fluorophenyl)benzaldehyde

O=Cc1ccccc1c1ccccc1F Request for Quotation
Chemical Name: 2-(2-fluorophenyl)benzaldehyde
CAS Number: 223575-95-9
Product Number: AG00BDYI(AGN-PC-0K4N52)
Synonyms:
MDL No:
Molecular Formula: C13H9FO
Molecular Weight: 200.2084

Identification/Properties

Computed Properties
Molecular Weight:
200.212g/mol
XLogP3:
3.1
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
200.064g/mol
Monoisotopic Mass:
200.064g/mol
Topological Polar Surface Area:
17.1A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
217
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2'-Fluoro-[1,1'-biphenyl]-2-carbaldehyde, commonly known as $name$, plays a crucial role in chemical synthesis as a versatile building block. This compound is utilized as a key intermediate in the synthesis of various organic molecules due to its unique structural properties and reactivity. In chemical synthesis, $name$ functions as a valuable starting material in the production of pharmaceuticals, agrochemicals, and advanced materials. Its distinct molecular structure provides opportunities for selective functionalization and modification, enabling chemists to design and create complex organic compounds with specific properties and functions. Additionally, the presence of the fluoro and aldehyde functional groups in $name$ allows for diverse reaction pathways and enables the incorporation of fluorine into target molecules, which can enhance biological activity and chemical stability. Overall, the strategic use of 2'-Fluoro-[1,1'-biphenyl]-2-carbaldehyde in chemical synthesis facilitates the efficient and controlled construction of diverse molecular architectures with potential applications in various industries.