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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-bromo-

N[C@@H](C(=O)O)Cc1c[nH]c2c1cc(Br)cc2 Request for Quotation
Chemical Name: D-Tryptophan, 5-bromo-
CAS Number: 93299-40-2
Product Number: AG00GUAT(AGN-PC-0ONLEB)
Synonyms:
MDL No:
Molecular Formula: C11H11BrN2O2
Molecular Weight: 283.1212

Identification/Properties

Properties
BP:
495.8±45.0°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
283.125g/mol
XLogP3:
-0.1
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
282g/mol
Monoisotopic Mass:
282g/mol
Topological Polar Surface Area:
79.1A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
275
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-bromo-1H-indol-3-yl)propanoic acid is a versatile compound commonly used in chemical synthesis due to its unique structure and reactivity. In chemical synthesis, this compound serves as a crucial building block for the creation of various organic molecules and pharmaceuticals. Its amino and indole functional groups make it an essential intermediate in the production of complex molecules. Specifically, the (R)-2-Amino-3-(5-bromo-1H-indol-3-yl)propanoic acid can be employed in the synthesis of chiral compounds, such as amino acids and peptide derivatives, where its stereochemistry plays a significant role in determining the properties and activities of the final products. Additionally, its bromoindole moiety allows for further derivatization and functionalization, expanding the potential applications of the synthesized molecules in drug development and organic chemistry research.