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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-Threonine, N-[(1,1-dimethylethoxy)carbonyl]-, phenylmethyl ester

C[C@H]([C@@H](C(=O)OCc1ccccc1)NC(=O)OC(C)(C)C)O C16H23NO5 Request for Quotation
Chemical Name: L-Threonine, N-[(1,1-dimethylethoxy)carbonyl]-, phenylmethyl ester
CAS Number: 33662-26-9
Product Number: AG00CJEG(AGN-PC-0O923P)
Synonyms:
MDL No:
Molecular Formula:
Molecular Weight:

Identification/Properties

Computed Properties
Molecular Weight:
309.362g/mol
XLogP3:
2.1
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
8
Exact Mass:
309.158g/mol
Monoisotopic Mass:
309.158g/mol
Topological Polar Surface Area:
84.9A^2
Heavy Atom Count:
22
Formal Charge:
0
Complexity:
371
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
2
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


Boc-Thr-OBzl is a compound widely utilized in chemical synthesis as a masked form of threonine. This Boc (tert-butyloxycarbonyl) protected threonine derivative is particularly valuable in peptide synthesis due to its stability and compatibility with a variety of chemical reactions. By using Boc-Thr-OBzl, chemists are able to selectively protect the threonine residue in a peptide chain, allowing for the synthesis of complex peptides and proteins with precise control over the sequence and structure. This compound finds application in the production of pharmaceuticals, bioconjugates, and other biologically relevant molecules, where the presence of threonine residues is crucial for the desired biological activity or function. Additionally, Boc-Thr-OBzl offers chemists a versatile tool for the modification and manipulation of peptide sequences, enabling the design and creation of novel compounds with tailored properties and activities.