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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-Fluoro-L-tryptophan monohydrate

N[C@H](C(=O)O)Cc1c[nH]c2c1cc(F)cc2 Request for Quotation
Chemical Name: 5-Fluoro-L-tryptophan monohydrate
CAS Number: 16626-02-1
Product Number: AG001WLJ(AGN-PC-0WAIMW)
Synonyms:
MDL No:
Molecular Formula: C11H11FN2O2
Molecular Weight: 222.2156

Identification/Properties

Computed Properties
Molecular Weight:
222.219g/mol
XLogP3:
-0.7
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:
1
Undefined Atom Stereocenter Count:
0
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:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The (S)-2-Amino-3-(5-fluoro-1H-indol-3-yl)propanoic acid is a valuable compound in chemical synthesis, particularly in the pharmaceutical industry. This molecule serves as a key building block for the preparation of various biologically active compounds and drug candidates. The presence of the fluoro-substituted indole moiety confers unique properties and reactivity to the molecule, making it a versatile intermediate in the development of novel pharmaceutical agents. By strategically incorporating this amino acid derivative into synthetic pathways, chemists can access a diverse array of structurally complex molecules with potential therapeutic applications.