BOC-SER(FMOC-GLY)-OH|944283-06-1,AngeneChemical

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Pyrimidine, 5-bromo-2-methyl-

1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide

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)-

BOC-SER(FMOC-GLY)-OH

O=C(CNC(=O)OCC1c2ccccc2c2c1cccc2)OC[C@@H](C(=O)O)NC(=O)OC(C)(C)C

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Chemical Name:	BOC-SER(FMOC-GLY)-OH
CAS Number:	944283-06-1
Product Number:	AG00VQXO(AGN-PC-0W40P6)
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Chemical Structure

In chemical synthesis, (S)-3-(2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)acetoxy)-2-((tert-butoxycarbonyl)amino)propanoic acid can serve as a versatile building block for creating complex molecules. Its unique structure allows for precise control over the stereochemistry of the resulting products, making it valuable for the synthesis of chiral compounds. By incorporating this compound into synthetic pathways, chemists can efficiently access a wide range of bioactive molecules, pharmaceuticals, and advanced materials with high purity and specificity.