1. Home
  2. 3’-Fluoro-4’-(1-pyrazolyl)acetophenone

Contact Angene

Tel: +852 8191 6999

Email: sales@angenechemical.com

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-4’-(1-pyrazolyl)acetophenone

Fc1cc(ccc1n1cccn1)C(=O)C Request for Quotation
Chemical Name: 3’-Fluoro-4’-(1-pyrazolyl)acetophenone
CAS Number: 1152964-31-2
Product Number: AG000GK2(AGN-PC-0WA7Y8)
Synonyms:
MDL No:
Molecular Formula: C11H9FN2O
Molecular Weight: 204.2004

Identification/Properties

Properties
Storage:
2-8℃;

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H320-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


The 3'-Fluoro-4'-(1-pyrazolyl)acetophenone is a versatile chemical reagent commonly used in chemical synthesis processes. It serves as a valuable building block in the creation of various pharmaceutical and agrochemical compounds due to its unique structural properties and reactivity. In synthetic chemistry, this compound is often employed as a key intermediate for the introduction of functional groups, such as the fluoro and pyrazolyl moieties, into complex molecular structures. Its application in the construction of heterocyclic compounds and the modification of aromatic systems makes it an essential tool for organic chemists seeking to design novel molecules with specific biological activities. Additionally, the 3'-Fluoro-4'-(1-pyrazolyl)acetophenone plays a crucial role in the development of drug candidates and advanced materials through controlled chemical transformations and strategic synthetic pathways.