1. Home
  2. Alpha-methyl-dl-tryptophan

Contact Angene

Tel: +852 8191 6999

Email: sales@angenechemical.com

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)-

Alpha-methyl-dl-tryptophan

OC(=O)C(Cc1c[nH]c2c1cccc2)(N)C Request for Quotation
Chemical Name: Alpha-methyl-dl-tryptophan
CAS Number: 153-91-3
Product Number: AG00382A(AGN-PC-0WACFL)
Synonyms:
MDL No:
Molecular Formula: C12H14N2O2
Molecular Weight: 218.2518

Identification/Properties

Computed Properties
Molecular Weight:
218.256g/mol
XLogP3:
-0.9
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:
282
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


Alpha-methyl-DL-tryptophan is a versatile compound used in chemical synthesis for constructing complex molecules with specific chirality and functional groups. This compound is particularly valuable in the development of pharmaceuticals, agrochemicals, and materials science due to its ability to serve as a key building block in the creation of novel organic compounds. By incorporating Alpha-methyl-DL-tryptophan into synthetic pathways, chemists can efficiently access a wide range of structurally diverse molecules, ultimately leading to advancements in drug discovery, materials design, and chemical research. Additionally, the unique structural features of Alpha-methyl-DL-tryptophan make it a valuable tool for studying enzyme-catalyzed reactions and investigating chiral recognition in biological systems. Its role in chemical synthesis extends beyond traditional organic chemistry and into the realms of bioorganic and medicinal chemistry, where the precise control of molecular structure is crucial for achieving desired biological activities and properties. Through innovative applications of Alpha-methyl-DL-tryptophan in chemical synthesis, researchers are pushing the boundaries of chemical discovery and uncovering new opportunities for addressing key challenges in various scientific fields.