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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)-

(3R)-3-amino-3-(2-fluorophenyl)propanoic acid

OC(=O)CC(c1ccccc1F)N Request for Quotation
Chemical Name: (3R)-3-amino-3-(2-fluorophenyl)propanoic acid
CAS Number: 117391-49-8
Product Number: AG000E7X(AGN-PC-0K5U4Y)
Synonyms:
MDL No: MFCD00193241
Molecular Formula: C9H10FNO2
Molecular Weight: 183.1796

Identification/Properties

Properties
MP:
222-224℃
BP:
302.6℃ at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
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-(2-fluorophenyl)propanoic acid, often referred to as $name$, is a versatile compound widely utilized in chemical synthesis due to its unique structural properties. This compound serves as a crucial building block in the creation of various pharmaceuticals, agrochemicals, and specialty chemicals. In the realm of chemical synthesis, $name$ plays a significant role in the production of diverse compounds through its ability to undergo various reactions and transformations.One key application of 3-Amino-3-(2-fluorophenyl)propanoic acid is in the pharmaceutical industry, where it serves as a precursor for the synthesis of different drug molecules. By incorporating this compound into specific reaction pathways, chemists can manipulate its structure to introduce desired functionalities and properties into the final pharmaceutical product. Additionally, the presence of the amino and fluorophenyl groups in $name$ enables the creation of complex molecules with enhanced biological activity and pharmacological effects.Furthermore, in agrochemical synthesis, the utilization of 3-Amino-3-(2-fluorophenyl)propanoic acid allows for the development of innovative pesticides, herbicides, and fertilizers. The chemical reactivity of this compound enables the construction of pesticide molecules with improved efficacy and selectivity, thus contributing to sustainable agricultural practices.Moreover, in the realm of specialty chemicals, the versatile nature of $name$ facilitates the production of a wide range of compounds used in various industrial applications. Its ability to participate in diverse chemical transformations, such as acylation, amidation, and condensation reactions, makes it a valuable component in the synthesis of specialty chemicals with tailored properties and functions.Overall, the application of 3-Amino-3-(2-fluorophenyl)propanoic acid in chemical synthesis underscores its importance as a foundational building block for the creation of pharmaceuticals, agrochemicals, and specialty chemicals with diverse applications across different industries.