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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-methoxyisonicotinaldehyde

COc1cncc(c1C=O)F Request for Quotation
Chemical Name: 3-Fluoro-5-methoxyisonicotinaldehyde
CAS Number: 1256792-34-3
Product Number: AG000OD8(AGN-PC-0WAGYI)
Synonyms:
MDL No:
Molecular Formula: C7H6FNO2
Molecular Weight: 155.1264

Identification/Properties

Computed Properties
Molecular Weight:
155.128g/mol
XLogP3:
0.4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
155.038g/mol
Monoisotopic Mass:
155.038g/mol
Topological Polar Surface Area:
39.2A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
142
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-methoxyisonicotinaldehyde is a versatile compound used extensively in chemical synthesis for its unique properties and reactivity. This compound serves as a key intermediate in the production of various pharmaceuticals, agrochemicals, and advanced materials. In chemical synthesis, 3-Fluoro-5-methoxyisonicotinaldehyde acts as a crucial building block for the creation of diverse molecular structures due to its functional groups and strategic placement of fluorine and methoxy substituents. Its presence in a synthesis pathway facilitates the formation of complex molecules by enabling selective reactions and functionalization processes. The reactivity of 3-Fluoro-5-methoxyisonicotinaldehyde allows for precise control over regioselectivity and stereoselectivity, leading to efficient and high-yield synthesis of target compounds. Researchers and chemists widely utilize this compound in the development of new pharmaceuticals, agrochemicals, and other specialty chemicals, highlighting its significance in advancing scientific research and industrial applications.