1. Home
  2. 1-(2-chloro-5-fluoropyridin-3-yl)ethanone

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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)-

1-(2-chloro-5-fluoropyridin-3-yl)ethanone

Fc1cnc(c(c1)C(=O)C)Cl Request for Quotation
Chemical Name: 1-(2-chloro-5-fluoropyridin-3-yl)ethanone
CAS Number: 1203499-12-0
Product Number: AG003CTN(AGN-PC-07R0J8)
Synonyms:
MDL No:
Molecular Formula: C7H5ClFNO
Molecular Weight: 173.5721

Identification/Properties

Properties
BP:
224.2±35.0°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


1-(2-Chloro-5-fluoropyridin-3-yl)ethanone is a versatile compound widely used in chemical synthesis, particularly in the pharmaceutical and agrochemical industries. This compound serves as a key building block for the preparation of various biologically active molecules, including pharmaceutical drugs and agricultural chemicals.One of the primary applications of 1-(2-Chloro-5-fluoropyridin-3-yl)ethanone is as a synthetic intermediate in the production of pyridine-based compounds. Pyridine derivatives are prevalent in pharmaceuticals due to their diverse biological activities and pharmacological properties. By utilizing 1-(2-Chloro-5-fluoropyridin-3-yl)ethanone as a starting material, chemists can efficiently access a wide range of substituted pyridine derivatives through sequential chemical transformations.Furthermore, this compound plays a crucial role in the synthesis of heterocyclic molecules, which are integral components of many pharmaceutical agents. The strategic incorporation of 1-(2-Chloro-5-fluoropyridin-3-yl)ethanone into chemical reactions allows for the construction of complex molecular structures with specific functional groups and stereochemistry, enabling the development of novel drug candidates and agrochemicals.Overall, the application of 1-(2-Chloro-5-fluoropyridin-3-yl)ethanone in chemical synthesis exemplifies its significance as a valuable tool for the efficient and versatile preparation of biologically active compounds with potential therapeutic and agricultural applications.