1. Home
  2. 4-(3-fluorophenyl)butan-2-amine

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)-

4-(3-fluorophenyl)butan-2-amine

CC(CCc1cccc(c1)F)N Request for Quotation
Chemical Name: 4-(3-fluorophenyl)butan-2-amine
CAS Number: 1092924-64-5
Product Number: AG01AITV(AG01AITV)
Synonyms:
MDL No:
Molecular Formula: C10H14FN
Molecular Weight: 167.2233

Identification/Properties

Computed Properties
Molecular Weight:
167.227g/mol
XLogP3:
2.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
3
Exact Mass:
167.111g/mol
Monoisotopic Mass:
167.111g/mol
Topological Polar Surface Area:
26A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
127
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
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

Request for Quotation

Customer Feedback

Chemical Structure


4-(3-Fluorophenyl)butan-2-amine is a versatile compound commonly utilized in chemical synthesis as a key building block in the production of various pharmaceuticals, agrochemicals, and fine chemicals. This compound serves as a crucial intermediate in the synthesis of bioactive molecules due to its unique structural features and functional groups.In chemical synthesis, 4-(3-Fluorophenyl)butan-2-amine can be effectively utilized in the preparation of diverse organic compounds through various synthetic routes. Its amine functional group offers opportunities for further modification through reactions such as reductive amination, N-alkylation, and reductive coupling, enabling the introduction of different bioactive moieties or structural motifs.Additionally, the presence of the fluorophenyl group in 4-(3-Fluorophenyl)butan-2-amine provides opportunities for directing regioselective reactions and facilitating specific molecular interactions in the target compounds. This fluorinated moiety can also impart favorable physicochemical properties to the final products, such as improved metabolic stability, enhanced binding affinity, or altered bioavailability.Overall, the strategic incorporation of 4-(3-Fluorophenyl)butan-2-amine in chemical synthesis enables the efficient construction of diverse molecular scaffolds with potential therapeutic or agricultural applications, highlighting its importance as a valuable building block in modern organic chemistry practices.