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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)-

L-Valine, N-[(1,1-dimethylethoxy)carbonyl]glycyl-

O=C(N[C@H](C(=O)O)C(C)C)CNC(=O)OC(C)(C)C Request for Quotation
Chemical Name: L-Valine, N-[(1,1-dimethylethoxy)carbonyl]glycyl-
CAS Number: 28334-73-8
Product Number: AG00I5BG(AGN-PC-0O8KIV)
Synonyms:
MDL No:
Molecular Formula: C12H22N2O5
Molecular Weight: 274.3135

Identification/Properties

Safety Information

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

NMR Spectrum

Other Analytical Data

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Chemical Structure


(S)-2-(2-((tert-Butoxycarbonyl)amino)acetamido)-3-methylbutanoic acid is a vital compound used in chemical synthesis, particularly in the field of peptide synthesis. This compound serves as a key building block for creating complex peptides with specific structural properties and functionalities.Due to its unique structure and reactivity, (S)-2-(2-((tert-Butoxycarbonyl)amino)acetamido)-3-methylbutanoic acid is commonly employed in solid-phase peptide synthesis (SPPS) and solution-phase peptide synthesis methods. Its amino acid derivative properties enable it to act as a crucial linker between other amino acids, facilitating the formation of peptide bonds and the sequential assembly of peptides in a controlled manner.Furthermore, the tert-Butoxycarbonyl (Boc) protective group attached to the amine group of the compound provides stability and protection during the peptide synthesis process. This protection allows for selective deprotection and enables the precise manipulation of the peptide chain, ensuring high yields and purity of the final peptide product.Overall, the application of (S)-2-(2-((tert-Butoxycarbonyl)amino)acetamido)-3-methylbutanoic acid in chemical synthesis plays a crucial role in the efficient and tailored production of peptides with diverse biological activities and potential therapeutic applications.