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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)-

5-(1-Fluoroethyl)-1H-pyrazol-3-amine

CC(c1cc(n[nH]1)N)F Request for Quotation
Chemical Name: 5-(1-Fluoroethyl)-1H-pyrazol-3-amine
CAS Number: 1451391-06-2
Product Number: AG001KM2(AGN-PC-0WAAOJ)
Synonyms:
MDL No:
Molecular Formula: C5H8FN3
Molecular Weight: 129.1355

Identification/Properties

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

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Chemical Structure


5-(1-Fluoroethyl)-1H-pyrazol-3-amine is a versatile compound commonly used in chemical synthesis. Its unique structure and reactivity make it an important building block in the development of various pharmaceuticals, agrochemicals, and materials.In organic synthesis, 5-(1-Fluoroethyl)-1H-pyrazol-3-amine serves as an essential intermediate for the preparation of biologically active compounds. It can undergo various functional group modifications, such as acylation, alkylation, and halogenation, leading to the formation of diverse molecular structures with desirable properties.Furthermore, this compound plays a crucial role in the development of novel drugs and therapeutics. By incorporating 5-(1-Fluoroethyl)-1H-pyrazol-3-amine into drug molecules, chemists can enhance their pharmacological activities, improve their bioavailability, and optimize their metabolic stability.Overall, the application of 5-(1-Fluoroethyl)-1H-pyrazol-3-amine in chemical synthesis offers a valuable toolbox for researchers in the fields of medicinal chemistry, material science, and agrochemical development. Its versatility and potential for molecular diversification make it a key component in the creation of innovative and impactful chemical compounds.