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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-Tyrosine, 3-hydroxy-, methyl ester, hydrochloride

COC(=O)[C@H](Cc1ccc(c(c1)O)O)N.Cl Request for Quotation
Chemical Name: L-Tyrosine, 3-hydroxy-, methyl ester, hydrochloride
CAS Number: 1421-65-4
Product Number: AG001HT2(AGN-PC-0O2DC2)
Synonyms:
MDL No:
Molecular Formula: C10H14ClNO4
Molecular Weight: 247.6755

Identification/Properties

Properties
MP:
174-175℃
Storage:
Inert atmosphere;-10 ℃;
Form:
Solid
Computed Properties
Molecular Weight:
247.675g/mol
Hydrogen Bond Donor Count:
4
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
4
Exact Mass:
247.061g/mol
Monoisotopic Mass:
247.061g/mol
Topological Polar Surface Area:
92.8A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
222
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


(S)-Methyl 2-amino-3-(3,4-dihydroxyphenyl)propanoate hydrochloride is an essential compound utilized in chemical synthesis for its versatile applications. This chiral molecule plays a crucial role in asymmetric synthesis, enabling the creation of enantiomerically pure compounds. Its presence is particularly valuable in the pharmaceutical industry, where the precise control of stereochemistry is paramount for drug development. By incorporating (S)-Methyl 2-amino-3-(3,4-dihydroxyphenyl)propanoate hydrochloride into synthetic pathways, chemists can efficiently access enantiomerically enriched products with high purity and specificity. Through strategic utilization in the synthesis of various pharmaceutical intermediates and active ingredients, this compound contributes significantly to advancing the field of medicinal chemistry and expanding the possibilities for targeted drug design.