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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)-

2-[(2-methylpropan-2-yl)oxycarbonylamino]-2-naphthalen-2-ylacetic acid

O=C(OC(C)(C)C)NC(c1ccc2c(c1)cccc2)C(=O)O Request for Quotation
Chemical Name: 2-[(2-methylpropan-2-yl)oxycarbonylamino]-2-naphthalen-2-ylacetic acid
CAS Number: 33741-79-6
Product Number: AG00CAOM(AGN-PC-00MDIR)
Synonyms:
MDL No: MFCD02683164
Molecular Formula: C17H19NO4
Molecular Weight: 301.33706

Identification/Properties

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-((tert-Butoxycarbonyl)amino)-2-(naphthalen-2-yl)acetic acid is a versatile compound commonly utilized in chemical synthesis as a protecting group for amino acids. In peptide synthesis, this compound plays a crucial role in safeguarding the amine group of amino acids by temporarily attaching the tert-butoxycarbonyl (Boc) protecting group, which prevents unwanted side reactions and selective reaction at specific sites. This protective group can be easily removed under mild conditions, allowing for further modifications or coupling reactions to take place without affecting other functional groups. The presence of the naphthalen-2-yl moiety provides additional stability and structural support to the molecule, making it a valuable tool in the synthesis of complex peptides and pharmaceutical compounds.