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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, 1-methyl-

OC(=O)[C@@H](Cc1cn(c2c1cccc2)C)N Request for Quotation
Chemical Name: D-Tryptophan, 1-methyl-
CAS Number: 110117-83-4
Product Number: AG0032T7(AGN-PC-0NXAXM)
Synonyms:
MDL No:
Molecular Formula: C12H14N2O2
Molecular Weight: 218.2518

Identification/Properties

Properties
MP:
242-245 °C
BP:
429.3 °C at 760 mmHg
Storage:
2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
218.256g/mol
XLogP3:
-1.3
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
218.106g/mol
Monoisotopic Mass:
218.106g/mol
Topological Polar Surface Area:
68.2A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
270
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


1-Methyl-D-tryptophan is a versatile compound used as a key building block in advanced chemical synthesis processes. Its unique structure and properties make it a valuable tool in creating a wide range of complex molecules with applications in pharmaceuticals, agrochemicals, and materials science. By incorporating 1-Methyl-D-tryptophan into various reaction schemes, chemists can access novel pathways to efficiently prepare intricate organic compounds with high purity and precision. This compound serves as a crucial intermediate in the synthesis of bioactive molecules, providing researchers with the opportunity to explore new avenues in drug discovery and development. In addition, its strategic placement within a molecular framework can influence the stereochemistry and bioactivity of the final products, offering tailored solutions for challenging synthetic targets. Whether utilized for probing enzymatic mechanisms or designing custom molecules, 1-Methyl-D-tryptophan exemplifies the ingenuity and limitless potential of modern chemical synthesis techniques.