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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)-

O-(2-Nitrobenzyl)-L-tyrosine Hydrochloride

OC(=O)[C@H](Cc1ccc(cc1)OCc1ccccc1[N+](=O)[O-])N.Cl Request for Quotation
Chemical Name: O-(2-Nitrobenzyl)-L-tyrosine Hydrochloride
CAS Number: 207727-86-4
Product Number: AG002J8U(AGN-PC-0WAEPT)
Synonyms:
MDL No: MFCD16495886
Molecular Formula: C16H17ClN2O5
Molecular Weight: 352.7696

Identification/Properties

Properties
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
352.771g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
6
Exact Mass:
352.083g/mol
Monoisotopic Mass:
352.083g/mol
Topological Polar Surface Area:
118A^2
Heavy Atom Count:
24
Formal Charge:
0
Complexity:
404
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:
2
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The (S)-2-Amino-3-(4-((2-nitrobenzyl)oxy)phenyl)propanoic acid hydrochloride serves as a crucial component in chemical synthesis processes, particularly in the realm of pharmaceuticals and fine chemicals production. As a versatile building block, this compound facilitates the creation of intricate molecular structures through its ability to participate in various key synthetic transformations.In chemical synthesis, (S)-2-Amino-3-(4-((2-nitrobenzyl)oxy)phenyl)propanoic acid hydrochloride can be utilized as a chiral starting material for the preparation of asymmetric compounds. Its unique stereochemical properties enable the controlled introduction of chirality into target molecules, a pivotal step in the synthesis of biologically active compounds and pharmaceutical intermediates.Furthermore, this compound plays a pivotal role in peptide synthesis as a critical intermediate in the formation of peptide bonds. By serving as a foundational unit in peptide assembly, it contributes to the construction of complex peptide structures with specific biological activities and functions.Overall, (S)-2-Amino-3-(4-((2-nitrobenzyl)oxy)phenyl)propanoic acid hydrochloride is an indispensable tool in the hands of synthetic chemists, enabling the efficient and strategic construction of diverse chemical entities with tailored properties and applications.