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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-Histidine, N-[(1,1-dimethylethoxy)carbonyl]-1-(phenylmethyl)-

OC(=O)[C@H](Cc1ncn(c1)Cc1ccccc1)NC(=O)OC(C)(C)C Request for Quotation
Chemical Name: L-Histidine, N-[(1,1-dimethylethoxy)carbonyl]-1-(phenylmethyl)-
CAS Number: 20898-44-6
Product Number: AG002JZC(AGN-PC-0O7OSQ)
Synonyms:
MDL No:
Molecular Formula: C18H23N3O4
Molecular Weight: 345.3929

Identification/Properties

Properties
MP:
181-184°C
BP:
572.1°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
345.399g/mol
XLogP3:
2.2
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
8
Exact Mass:
345.169g/mol
Monoisotopic Mass:
345.169g/mol
Topological Polar Surface Area:
93.4A^2
Heavy Atom Count:
25
Formal Charge:
0
Complexity:
458
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


Boc-His(Bzl)-OH is a commonly used building block in chemical synthesis, particularly in peptide synthesis. It serves as a protected form of histidine, a versatile amino acid with both acidic and basic properties. The Boc (tert-butoxycarbonyl) protecting group on the amino terminus of histidine provides stability to the molecule during chemical reactions, allowing for selective manipulation of other functional groups without affecting the histidine residue. This enables chemists to control the sequence of amino acids in a peptide chain and ultimately determine the structure and function of the resulting peptide. Boc-His(Bzl)-OH is utilized in the synthesis of various peptide-based pharmaceuticals, research chemicals, and bioconjugates, making it an essential tool in the field of organic chemistry.