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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)-

Carbamic acid,[(1S)-2-[(2,5-dioxo-1-pyrrolidinyl)oxy]-1-[(4-hydroxyphenyl)methyl]-2-oxoethyl]-, 1,1-dimethylethyl ester

O=C([C@H](Cc1ccc(cc1)O)NC(=O)OC(C)(C)C)ON1C(=O)CCC1=O Request for Quotation
Chemical Name: Carbamic acid,[(1S)-2-[(2,5-dioxo-1-pyrrolidinyl)oxy]-1-[(4-hydroxyphenyl)methyl]-2-oxoethyl]-, 1,1-dimethylethyl ester
CAS Number: 20866-56-2
Product Number: AG003OIH(AGN-PC-0QWP2P)
Synonyms:
MDL No:
Molecular Formula: C18H22N2O7
Molecular Weight: 378.3765

Identification/Properties

Properties
MP:
~190 °C (dec.)
Storage:
2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
378.381g/mol
XLogP3:
1.6
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
7
Rotatable Bond Count:
8
Exact Mass:
378.143g/mol
Monoisotopic Mass:
378.143g/mol
Topological Polar Surface Area:
122A^2
Heavy Atom Count:
27
Formal Charge:
0
Complexity:
575
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
1
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-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


Boc-Tyr-OSu, known chemically as Nα-tert-butoxycarbonyl-L-tyrosine N-hydroxysuccinimide ester, is a valuable reagent used in chemical synthesis for the selective functionalization of tyrosine residues in peptides and proteins. In peptide chemistry, Boc-Tyr-OSu is commonly employed for the introduction of a tert-butoxycarbonyl (Boc) protecting group on the side chain of tyrosine. This protection strategy is crucial for controlling the reactivity and specificity of subsequent chemical reactions in peptide synthesis. Furthermore, the N-hydroxysuccinimide ester moiety in Boc-Tyr-OSu facilitates the coupling of the tyrosine residue to other amino acids or molecules, enabling the formation of peptide bonds and peptide conjugates with high efficiency. With its versatility and reliability, Boc-Tyr-OSu plays a pivotal role in the precise construction of peptide sequences and the development of diverse peptide-based compounds for various research and pharmaceutical applications.