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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)-

Glycine, L-tryptophyl-

OC(=O)CNC(=O)[C@H](Cc1c[nH]c2c1cccc2)N Request for Quotation
Chemical Name: Glycine, L-tryptophyl-
CAS Number: 7360-09-0
Product Number: AG008QMG(AGN-PC-0OHB1I)
Synonyms:
MDL No:
Molecular Formula: C13H15N3O3
Molecular Weight: 261.2765

Identification/Properties

Computed Properties
Molecular Weight:
261.281g/mol
XLogP3:
-2.1
Hydrogen Bond Donor Count:
4
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
5
Exact Mass:
261.111g/mol
Monoisotopic Mass:
261.111g/mol
Topological Polar Surface Area:
108A^2
Heavy Atom Count:
19
Formal Charge:
0
Complexity:
348
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


(S)-2-(2-Amino-3-(1H-indol-3-yl)propanamido)acetic acid is a versatile compound that finds its application in chemical synthesis as a key building block for the preparation of various pharmaceuticals and biologically active molecules. Its unique structure allows it to participate in diverse reactions, making it a valuable intermediate in organic synthesis.One of the key applications of (S)-2-(2-Amino-3-(1H-indol-3-yl)propanamido)acetic acid is in the synthesis of peptide derivatives. Peptides are important molecules in drug discovery and development, as they play a crucial role in various biological processes. By incorporating this compound into peptide synthesis, chemists can introduce specific functionalities and enhance the bioactivity of the resulting peptides.Furthermore, (S)-2-(2-Amino-3-(1H-indol-3-yl)propanamido)acetic acid can be used in the preparation of chiral compounds. As it contains a chiral center, this compound enables the synthesis of enantiomerically pure molecules, which are essential in the pharmaceutical industry where the stereochemistry of a molecule can significantly impact its biological activity and pharmacokinetic properties.Overall, the versatile nature of (S)-2-(2-Amino-3-(1H-indol-3-yl)propanamido)acetic acid makes it a valuable tool in chemical synthesis for the development of novel pharmaceuticals, bioactive molecules, and chiral compounds.