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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)-

3-O-Methyl-L-DOPA Monohydrate

COc1cc(ccc1O)C[C@@H](C(=O)O)N.O Request for Quotation
Chemical Name: 3-O-Methyl-L-DOPA Monohydrate
CAS Number: 200630-46-2
Product Number: AG00C2PD(AGN-PC-0WAG0U)
Synonyms:
MDL No:
Molecular Formula: C10H15NO5
Molecular Weight: 229.2298

Identification/Properties

Computed Properties
Molecular Weight:
229.232g/mol
Hydrogen Bond Donor Count:
4
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
4
Exact Mass:
229.095g/mol
Monoisotopic Mass:
229.095g/mol
Topological Polar Surface Area:
93.8A^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


3-Methoxy-L-tyrosine monohydrate, also known as Meta-Oxy Tyrosine, plays a crucial role in chemical synthesis as a key intermediate compound. Its unique structure and properties make it an invaluable component in the production of various organic compounds and pharmaceutical agents. In chemical synthesis, 3-Methoxy-L-tyrosine monohydrate serves as a versatile building block for creating complex molecules with specific functionalities. Its incorporation into synthetic pathways enables the formation of novel structures and the modification of existing chemical entities, enhancing the diversity and utility of chemical compounds in research and industrial applications. This compound's involvement in chemical synthesis extends beyond its intrinsic properties, serving as a strategic tool for chemists to design and develop advanced materials, pharmaceuticals, and agrochemicals with enhanced properties and performance. Whether utilized as a precursor, reagent, or catalyst, 3-Methoxy-L-tyrosine monohydrate proves indispensable in advancing chemical synthesis towards the discovery of innovative solutions and breakthrough products.