1. Home
  2. EthylL-tyrosinate

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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)-

EthylL-tyrosinate

CCOC(=O)[C@H](Cc1ccc(cc1)O)N Request for Quotation
Chemical Name: EthylL-tyrosinate
CAS Number: 949-67-7
Product Number: AG003RDL(AGN-PC-0WADB5)
Synonyms:
MDL No:
Molecular Formula: C11H15NO3
Molecular Weight: 209.2417

Identification/Properties

Properties
MP:
103 °C
BP:
343.3°C at 760 mmHg
Storage:
Keep in dry area;-10 ℃;
Form:
Solid
Refractive Index:
17.5 ° (C=5, EtOH)
Computed Properties
Molecular Weight:
209.245g/mol
XLogP3:
0.6
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
5
Exact Mass:
209.105g/mol
Monoisotopic Mass:
209.105g/mol
Topological Polar Surface Area:
72.6A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
200
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

Request for Quotation

Customer Feedback

Chemical Structure


L-Tyrosine ethyl ester is a versatile compound commonly utilized in chemical synthesis for a wide range of applications. As a derivative of the amino acid L-Tyrosine, this ethyl ester variant offers enhanced solubility and stability compared to its parent compound. In organic chemistry, L-Tyrosine ethyl ester serves as a valuable building block for the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals. Its reactivity and compatibility with various functional groups make it a valuable precursor in the production of peptide conjugates and prodrugs. Additionally, L-Tyrosine ethyl ester is often employed as a chiral auxiliary in asymmetric synthesis, enabling the formation of enantiomerically pure compounds. Its unique properties and versatility make it a valuable tool in the hands of synthetic chemists seeking to create novel molecules with tailored functionalities.