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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-ethynyl-5-fluoro-3-methylpyridine

C#Cc1ncc(cc1C)F Request for Quotation
Chemical Name: 2-ethynyl-5-fluoro-3-methylpyridine
CAS Number: 1372103-93-9
Product Number: AG009EXB(AGN-PC-0WNWA4)
Synonyms:
MDL No:
Molecular Formula: C8H6FN
Molecular Weight: 135.1383

Identification/Properties

Computed Properties
Molecular Weight:
135.141g/mol
XLogP3:
1.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
135.048g/mol
Monoisotopic Mass:
135.048g/mol
Topological Polar Surface Area:
12.9A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
158
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


2-Ethynyl-5-Fluoro-3-Methylpyridine, also known as EFMP, is a versatile compound widely used in chemical synthesis due to its unique properties and reactivity. One key application of EFMP is as a building block in the synthesis of various pharmaceuticals and agrochemicals. Its alkyne functional group allows for efficient derivatization and the creation of diverse molecular architectures. Additionally, the presence of a fluorine atom enhances the compound's bioavailability and metabolic stability, making it an attractive candidate for drug discovery and development. In organic synthesis, EFMP serves as a valuable starting material for the construction of heterocyclic compounds and complex organic molecules. Its strategic placement of functional groups enables selective cross-coupling reactions, cyclization processes, and formation of carbon-carbon bonds, facilitating the efficient synthesis of target molecules with high structural diversity and biological activity. Overall, the use of 2-Ethynyl-5-Fluoro-3-Methylpyridine in chemical synthesis plays a crucial role in the advancement of medicinal and agricultural chemistry, offering a powerful tool for the creation of novel compounds with potential therapeutic and pesticidal properties.