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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)-

3-(5-chloro-1H-indol-3-yl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid

OC(=O)C(Cc1c[nH]c2c1cc(Cl)cc2)NC(=O)OC(C)(C)C Request for Quotation
Chemical Name: 3-(5-chloro-1H-indol-3-yl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid
CAS Number: 361576-61-6
Product Number: AG003OFL(AGN-PC-03NRZB)
Synonyms:
MDL No: MFCD09264328
Molecular Formula: C16H19ClN2O4
Molecular Weight: 338.7861

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H317
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


Boc-5-chloro-DL-tryptophan is a valuable compound utilized in chemical synthesis as a versatile building block. Its unique structure and reactivity make it particularly useful in the production of various pharmaceuticals, agrochemicals, and specialty chemicals. This compound is commonly employed as a key intermediate in the synthesis of complex molecules due to its ability to introduce functional groups with precision and control. By incorporating Boc-5-chloro-DL-tryptophan into synthetic pathways, chemists can tailor the molecular architecture of their desired products, enabling the synthesis of diverse chemical entities with specific biological activities or physical properties. Additionally, the protected nature of the Boc (tert-butoxycarbonyl) group in Boc-5-chloro-DL-tryptophan ensures stability during reactions, facilitating the manipulation of the compound under various conditions. Overall, the strategic use of Boc-5-chloro-DL-tryptophan in chemical synthesis enables researchers to access a wide range of structurally complex molecules for applications in drug discovery, material science, and beyond.