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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)-

2-amino-3-(4-fluoro-1H-indol-3-yl)propanoic acid

OC(=O)C(Cc1c[nH]c2c1c(F)ccc2)N Request for Quotation
Chemical Name: 2-amino-3-(4-fluoro-1H-indol-3-yl)propanoic acid
CAS Number: 25631-05-4
Product Number: AG00BD49(AGN-PC-0JLCNJ)
Synonyms:
MDL No:
Molecular Formula:
Molecular Weight:

Identification/Properties

Properties
BP:
450.7°C at 760 mmHg
Storage:
Inert atmosphere;-10 ℃;
Form:
Solid
Computed Properties
Molecular Weight:
222.219g/mol
XLogP3:
-1.1
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
222.08g/mol
Monoisotopic Mass:
222.08g/mol
Topological Polar Surface Area:
79.1A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
275
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

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Chemical Structure


2-Amino-3-(4-fluoro-1H-indol-3-yl)propanoic acid, commonly known as $name$, is a versatile compound frequently utilized in chemical synthesis. This compound plays a crucial role in organic chemistry as a key building block for the creation of various pharmaceuticals, agrochemicals, and materials.In chemical synthesis, $name$ serves as a valuable intermediate in the production of diverse compounds due to its unique structure and reactivity. By incorporating $name$ into a synthetic pathway, chemists can introduce the crucial indole ring and amino acid functionality into target molecules, allowing for the modification of properties such as biological activity, solubility, and stability.Furthermore, the presence of the fluoro substituent on the indole ring enhances the compound's pharmacokinetic properties and can impart specific interactions with biological targets. This opens up opportunities for the design and development of novel drug candidates with improved potency and selectivity.Overall, the application of 2-Amino-3-(4-fluoro-1H-indol-3-yl)propanoic acid in chemical synthesis highlights its significance as a versatile and strategic building block in the construction of complex molecules with potential applications in various industries.