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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)-

(2S)-2-amino-3-(7-methyl-1H-indol-3-yl)propanoic acid

Cc1cccc2c1[nH]cc2C[C@@H](C(=O)O)N Request for Quotation
Chemical Name: (2S)-2-amino-3-(7-methyl-1H-indol-3-yl)propanoic acid
CAS Number: 17332-70-6
Product Number: AG001YSN(AGN-PC-00NRIW)
Synonyms:
MDL No:
Molecular Formula: C12H14N2O2
Molecular Weight: 218.2518

Identification/Properties

Computed Properties
Molecular Weight:
218.256g/mol
XLogP3:
-0.7
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
218.106g/mol
Monoisotopic Mass:
218.106g/mol
Topological Polar Surface Area:
79.1A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
270
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#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Amino-3-(7-methyl-1H-indol-3-yl)propanoic acid is a versatile compound commonly employed in chemical synthesis for its unique reactivity and potential applications. This specialized amino acid derivative plays a crucial role in the development of novel pharmaceuticals, agrochemicals, and materials science. Its strategic incorporation into synthetic pathways enables the introduction of specific functional groups, thereby facilitating the generation of complex and structurally diverse molecules. By serving as a key building block, this compound acts as a valuable tool for organic chemists seeking to design and produce cutting-edge compounds with enhanced properties and biological activities.