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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)-

D-Tryptophan, 5-methoxy-

COc1ccc2c(c1)c(c[nH]2)C[C@H](C(=O)O)N Request for Quotation
Chemical Name: D-Tryptophan, 5-methoxy-
CAS Number: 89496-02-6
Product Number: AG0041WE(AGN-PC-0OM549)
Synonyms:
MDL No:
Molecular Formula: C12H14N2O3
Molecular Weight: 234.2512

Identification/Properties

Computed Properties
Molecular Weight:
234.255g/mol
XLogP3:
-0.8
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
234.1g/mol
Monoisotopic Mass:
234.1g/mol
Topological Polar Surface Area:
88.3A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
285
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#:
N/A
Hazard Statements:
H302-H317
Precautionary Statements:
P280
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


The (R)-2-Amino-3-(5-methoxy-1H-indol-3-yl)propanoic acid, commonly known as $name$, serves as a valuable building block in chemical synthesis due to its unique structural properties. This compound is frequently utilized in the preparation of various pharmaceuticals, agrochemicals, and functional materials. Specifically, $name$ is employed in the synthesis of diverse drug candidates, such as anticancer agents, antimicrobial compounds, and central nervous system drugs.In chemical synthesis, (R)-2-Amino-3-(5-methoxy-1H-indol-3-yl)propanoic acid acts as a key intermediate for the formation of complex molecules with specific biological activities. It participates in multistep reactions to introduce essential functional groups and stereocenters, enabling the production of chirally pure compounds essential for drug development. Furthermore, its indole moiety confers aromatic and heterocyclic characteristics, making it a versatile scaffold for the construction of diverse chemical structures.The use of (R)-2-Amino-3-(5-methoxy-1H-indol-3-yl)propanoic acid in chemical synthesis highlights its significance in creating novel organic molecules with promising pharmacological properties. Incorporating this compound into synthetic pathways enables the efficient construction of intricate molecular frameworks essential for expanding the chemical space of potential drug candidates and bioactive compounds.