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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)-

1,2,4-Piperazinetricarboxylic acid, 4-(1,1-dimethylethyl)1-(phenylmethyl) ester, (2S)-

[O-]C(=O)[C@@H]1CN(CCN1C(=O)OCc1ccccc1)C(=O)OC(C)(C)C Request for Quotation
Chemical Name: 1,2,4-Piperazinetricarboxylic acid, 4-(1,1-dimethylethyl)1-(phenylmethyl) ester, (2S)-
CAS Number: 150407-69-5
Product Number: AG001MLA(AGN-PC-0Q4PAS)
Synonyms:
MDL No:
Molecular Formula: C18H23N2O6-
Molecular Weight: 363.3850

Identification/Properties

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


(S)-1-((Benzyloxy)carbonyl)-4-(tert-butoxycarbonyl)piperazine-2-carboxylic acid, also known as $name$, is a valuable compound in chemical synthesis. This compound is commonly used as a protecting group in organic chemistry reactions. By selectively masking certain functional groups within a molecule, this compound allows chemists to target specific reactions without interfering with other parts of the molecule.In chemical synthesis, (S)-1-((Benzyloxy)carbonyl)-4-(tert-butoxycarbonyl)piperazine-2-carboxylic acid is often employed to protect the amine group of a molecule. This protection is essential in order to prevent unwanted side reactions or interactions during subsequent steps in a synthesis sequence. Once the desired reactions are completed, the protecting group can be easily removed, revealing the free amine group for further modifications or reactions.Overall, the application of (S)-1-((Benzyloxy)carbonyl)-4-(tert-butoxycarbonyl)piperazine-2-carboxylic acid in chemical synthesis provides chemists with a versatile tool to control the reactivity of molecules and achieve specific goals in complex organic transformations.