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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)-

(S)-1-Benzyl 5-tert-butyl 2-aminopentanedioate hydrochloride

O=C(OC(C)(C)C)CC[C@@H](C(=O)OCc1ccccc1)N.Cl Request for Quotation
Chemical Name: (S)-1-Benzyl 5-tert-butyl 2-aminopentanedioate hydrochloride
CAS Number: 98102-32-0
Product Number: AG00IK15(AGN-PC-0WAIL3)
Synonyms:
MDL No:
Molecular Formula: C16H24ClNO4
Molecular Weight: 329.8191

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Chemical Structure


In chemical synthesis, H-Glu(OtBu)-OBzl.HCl is commonly used as a reagent for peptide bond formation. It serves as a protected form of glutamic acid, an essential amino acid, allowing for controlled reactions during peptide assembly. The t-butoxycarbonyl (OtBu) and benzyl (OBzl) protecting groups on the glutamic acid ensure selectivity and prevent unwanted side reactions. By adding H-Glu(OtBu)-OBzl.HCl to the reaction mixture, chemists can facilitate the formation of specific peptide bonds with high precision and efficiency. This reagent plays a crucial role in the synthesis of complex peptides and organic molecules with glutamic acid residues, enabling the creation of diverse and intricate molecular structures for various scientific and pharmaceutical applications.