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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)-

3-amino-3-(3-fluorophenyl)propanoic acid

OC(=O)CC(c1cccc(c1)F)N Request for Quotation
Chemical Name: 3-amino-3-(3-fluorophenyl)propanoic acid
CAS Number: 117391-51-2
Product Number: AG000E7V(AGN-PC-0JT8A3)
Synonyms:
MDL No: MFCD00764457
Molecular Formula: C9H10FNO2
Molecular Weight: 183.1796

Identification/Properties

Computed Properties
Molecular Weight:
183.182g/mol
XLogP3:
-1.9
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
183.07g/mol
Monoisotopic Mass:
183.07g/mol
Topological Polar Surface Area:
63.3A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
187
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

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

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-Amino-3-(3-Fluorophenyl)Propanoic Acid, also known as $name$, serves a crucial role in chemical synthesis as a versatile building block. Its unique chemical structure allows for a wide range of applications in the synthesis of various pharmaceuticals, agrochemicals, and materials.In chemical synthesis, $name$ can be used as a key intermediate in the production of complex organic compounds. Its amino and fluorophenyl functional groups make it a valuable reagent for creating diverse molecular structures through multistep synthesis processes. Additionally, the presence of a propanoic acid moiety provides opportunities for further derivatization and modification, enhancing the versatility of this compound in the creation of novel chemical entities.Furthermore, the specific properties of 3-Amino-3-(3-Fluorophenyl)Propanoic Acid make it a favored choice in the development of pharmaceuticals with potential therapeutic benefits. Its ability to participate in various chemical reactions and form stable intermediates enables the efficient synthesis of bioactive compounds that target specific biological pathways or molecular targets.Overall, the application of 3-Amino-3-(3-Fluorophenyl)Propanoic Acid in chemical synthesis extends beyond mere reactions; it represents a fundamental building block that contributes to the advancement of drug discovery, material science, and other interdisciplinary fields.