949-67-7,MFCD00063046
Catalog No.:AA003RAT

949-67-7 | L-Tyrosine ethyl ester

Pack Size
Purity
Availability
Price(USD)
Quantity
  
5g
98%
in stock  
$29.00   $20.00
- +
25g
98%
in stock  
$54.00   $38.00
- +
100g
98%
in stock  
$130.00 $91.00
  • Technical Information
  • Properties
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA003RAT
Chemical Name:
L-Tyrosine ethyl ester
CAS Number:
949-67-7
Molecular Formula:
C11H15NO3
Molecular Weight:
209.2417
MDL Number:
MFCD00063046
SMILES:
CCOC(=O)[C@H](Cc1ccc(cc1)O)N
Properties
Properties
 
BP:
343.3°C at 760 mmHg  
Form:
Solid  
MP:
103 °C  
Refractive Index:
17.5 ° (C=5, EtOH)  
Storage:
Keep in dry area;-20 ℃;  

Computed Properties
 
Complexity:
200  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
1  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
15  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0  
Rotatable Bond Count:
5  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
0.6  

Literature

Title: Dimorphism of the prodrug L-tyrosine ethyl ester: pressure-temperature state diagram and crystal structure of phase II.

Journal: Journal of pharmaceutical sciences 20111101

Title: Synthesis and evaluation of amino acid-based radiotracer 99mTc-N4-AMT for breast cancer imaging.

Journal: Journal of biomedicine & biotechnology 20110101

Title: High level production of bioactive di- and tri-tyrosine peptides by protease-catalyzed reactions.

Journal: Journal of biotechnology 20101101

Title: Probing molecular motion by double-quantum (13C,13C) solid-state NMR spectroscopy: application to ubiquitin.

Journal: Journal of the American Chemical Society 20100113

Title: Singlet molecular oxygen [O2(1Deltag)]-mediated photodegradation of tyrosine derivatives in the presence of cationic and neutral micellar systems.

Journal: Amino acids 20080601

Title: Synthesis of gossypol atropisomers and derivatives and evaluation of their anti-proliferative and anti-oxidant activity.

Journal: Bioorganic & medicinal chemistry 20050701

Title: Transverse dephasing optimised NMR spectroscopy in solids: natural-abundance 13C correlation spectra.

Journal: Chemphyschem : a European journal of chemical physics and physical chemistry 20040621

Title: Fluorescence spectroscopic study of alpha-chymotrypsin relevant to the enantioselectivity for optical resolution of amino acid esters in organic solvents.

Journal: Biotechnology letters 20040401

Title: Light-driven tyrosine radical formation in a ruthenium-tyrosine complex attached to nanoparticle TiO2.

Journal: Inorganic chemistry 20021202

Title: Synthesis of 2-[18F]fluoro-L-tyrosine via regiospecific fluoro-de-stannylation.

Journal: Applied radiation and isotopes : including data, instrumentation and methods for use in agriculture, industry and medicine 20020801

Title: Approaches to the synthesis of some tyrosine-derived marine sponge metabolites: synthesis of verongamine and purealidin N.

Journal: The Journal of organic chemistry 20010504

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SDS
Tags:949-67-7 Molecular Formula|949-67-7 MDL|949-67-7 SMILES|949-67-7 L-Tyrosine ethyl ester
Catalog No.: AA003RAT
949-67-7,MFCD00063046
949-67-7 | L-Tyrosine ethyl ester
Pack Size: 5g
Purity: 98%
in stock
$29.00 $20.00
Pack Size: 25g
Purity: 98%
in stock
$54.00 $38.00
Pack Size: 100g
Purity: 98%
in stock
$130.00 $91.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA003RAT
Chemical Name: L-Tyrosine ethyl ester
CAS Number: 949-67-7
Molecular Formula: C11H15NO3
Molecular Weight: 209.2417
MDL Number: MFCD00063046
SMILES: CCOC(=O)[C@H](Cc1ccc(cc1)O)N
Properties
BP: 343.3°C at 760 mmHg  
Form: Solid  
MP: 103 °C  
Refractive Index: 17.5 ° (C=5, EtOH)  
Storage: Keep in dry area;-20 ℃;  
Complexity: 200  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 1  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 15  
Hydrogen Bond Acceptor Count: 4  
Hydrogen Bond Donor Count: 2  
Isotope Atom Count: 0  
Rotatable Bond Count: 5  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: 0.6  
Literature fold

Title: Dimorphism of the prodrug L-tyrosine ethyl ester: pressure-temperature state diagram and crystal structure of phase II.

Journal: Journal of pharmaceutical sciences20111101

Title: Synthesis and evaluation of amino acid-based radiotracer 99mTc-N4-AMT for breast cancer imaging.

Journal: Journal of biomedicine & biotechnology20110101

Title: High level production of bioactive di- and tri-tyrosine peptides by protease-catalyzed reactions.

Journal: Journal of biotechnology20101101

Title: Probing molecular motion by double-quantum (13C,13C) solid-state NMR spectroscopy: application to ubiquitin.

Journal: Journal of the American Chemical Society20100113

Title: Singlet molecular oxygen [O2(1Deltag)]-mediated photodegradation of tyrosine derivatives in the presence of cationic and neutral micellar systems.

Journal: Amino acids20080601

Title: Synthesis of gossypol atropisomers and derivatives and evaluation of their anti-proliferative and anti-oxidant activity.

Journal: Bioorganic & medicinal chemistry20050701

Title: Transverse dephasing optimised NMR spectroscopy in solids: natural-abundance 13C correlation spectra.

Journal: Chemphyschem : a European journal of chemical physics and physical chemistry20040621

Title: Fluorescence spectroscopic study of alpha-chymotrypsin relevant to the enantioselectivity for optical resolution of amino acid esters in organic solvents.

Journal: Biotechnology letters20040401

Title: Light-driven tyrosine radical formation in a ruthenium-tyrosine complex attached to nanoparticle TiO2.

Journal: Inorganic chemistry20021202

Title: Synthesis of 2-[18F]fluoro-L-tyrosine via regiospecific fluoro-de-stannylation.

Journal: Applied radiation and isotopes : including data, instrumentation and methods for use in agriculture, industry and medicine20020801

Title: Approaches to the synthesis of some tyrosine-derived marine sponge metabolites: synthesis of verongamine and purealidin N.

Journal: The Journal of organic chemistry20010504

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