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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)-

Tyrosine, a-methyl-, methyl ester, hydrochloride

COC(=O)C(Cc1ccc(cc1)O)(N)C.Cl Request for Quotation
Chemical Name: Tyrosine, a-methyl-, methyl ester, hydrochloride
CAS Number: 7361-31-1
Product Number: AG003NSB(AGN-PC-0U3DP5)
Synonyms:
MDL No:
Molecular Formula: C11H16ClNO3
Molecular Weight: 245.7026

Identification/Properties

Properties
MP:
192 °C (dec.)(lit.)
Storage:
Inert atmosphere;-10 ℃;
Form:
Solid
Solubility:
H2O: 50 mg/mL, clear, faintly yellow
Computed Properties
Molecular Weight:
245.703g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
245.082g/mol
Monoisotopic Mass:
245.082g/mol
Topological Polar Surface Area:
72.6A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
224
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
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


Methyl 2-amino-3-(4-hydroxyphenyl)-2-methylpropanoate hydrochloride plays a crucial role in chemical synthesis as a versatile building block. This compound is commonly utilized in the development of pharmaceuticals, agrochemicals, and functional materials. With its unique chemical structure, this compound acts as a key intermediate in the synthesis of various bioactive molecules, especially those with therapeutic properties. Its presence facilitates the incorporation of specific functional groups that are essential for enhancing the efficacy and specificity of the final products. Researchers and chemists often rely on Methyl 2-amino-3-(4-hydroxyphenyl)-2-methylpropanoate hydrochloride for its remarkable reactivity and compatibility in complex synthetic pathways, making it an indispensable tool in the realm of chemical innovation.