o-Ethyl-d-tyrosine

Base Information

Chemical Name:o-Ethyl-d-tyrosine
CAS No.:127419-60-7
Molecular Formula:C11H15NO3
Molecular Weight:209.245
Hs Code.:
UNII:IG65NW7N2O
Mol file:127419-60-7.mol

Synonyms:o-ethyl-d-tyrosine;127419-60-7;D-Tyrosine, O-ethyl- (9CI);(2R)-2-amino-3-(4-ethoxyphenyl)propanoic acid;(R)-2-amino-3-(4-ethoxyphenyl)propanoic acid;D-Tyrosine, O-ethyl-;IG65NW7N2O;3-(p-Ethoxyphenyl)-D-alanine;DTyr(Et);D-Tyr(Et);(O-ethyl)-d-tyrosine;UNII-IG65NW7N2O;SCHEMBL2036599;RMYPEYHEPIZYDJ-SNVBAGLBSA-N;AC8611;AKOS017482243;CS-0334595;(R)-2-amino-3-(4-ethoxyphenyl)propanoicacid;(R)-2-Amino-3-(4-ethoxy-phenyl)-propionic acid

Suppliers and Price of o-Ethyl-d-tyrosine

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

AK Scientific
o-Ethyl-d-tyrosine
1g
$ 863.00

Activate Scientific
O-Ethyl-D-tyrosine 95% ee
25 g
$ 1273.00

Activate Scientific
O-Ethyl-D-tyrosine 95% ee
1 g
$ 149.00

Activate Scientific
O-Ethyl-D-tyrosine 95% ee
5 g
$ 458.00

Acrotein
O-Ethyl-D-tyrosine 97%
5g
$ 330.00

Acrotein
O-Ethyl-D-tyrosine 97%
1g
$ 110.00

Total 5 raw suppliers

Chemical Property of o-Ethyl-d-tyrosine

Chemical Property:

Boiling Point:362.3±32.0 °C(Predicted)
PKA:2.24±0.10(Predicted)
PSA：72.55000
Density:1.175±0.06 g/cm3(Predicted)
LogP:1.74000
XLogP3:-0.8
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:5
Exact Mass:209.10519334
Heavy Atom Count:15
Complexity:200

Purity/Quality:

>98% ^*data from raw suppliers

o-Ethyl-d-tyrosine ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCOC1=CC=C(C=C1)CC(C(=O)O)N
Isomeric SMILES:CCOC1=CC=C(C=C1)C[C@H](C(=O)O)N

Technology Process of o-Ethyl-d-tyrosine

There total 1 articles about o-Ethyl-d-tyrosine which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 100.0%

: 76757-92-1,247088-44-4
(R)-2-((tert-butoxycarbonyl)amino)-3-(4-ethoxyphenyl)propanoic acid

: 127419-60-7,3909-20-4,748068-32-8
(R)-2-amino-3-(4-ethoxy-phenyl)-propionic acid

Guidance literature:: With hydrogenchloride; In 1,4-dioxane; at 20 ℃; for 1h;

Reference yield: 90.0%

: 127419-60-7,3909-20-4,748068-32-8
(R)-2-amino-3-(4-ethoxy-phenyl)-propionic acid

: 501-53-1,94274-21-2
benzyl chloroformate

: 561041-07-4
(R)-2-benzyloxycarbonylamino-3-(4-ethoxy-phenyl)-propionic acid

Guidance literature:: With sodium hydroxide; In 1,4-dioxane; water; at 20 ℃; for 18h;

Reference yield:

: 127419-60-7,3909-20-4,748068-32-8
(R)-2-amino-3-(4-ethoxy-phenyl)-propionic acid

: 1417694-08-6
N-[(R)-1-[(S)-1-(4-aminomethyl-benzylcarbamoyl)-2-phenyl-ethylcarbamoyl]-2-(4-ethoxy-phenyl)-ethyl]-benzamide hydrochloride

Guidance literature:: Multi-step reaction with 5 steps

1: sodium hydroxide / water; 1,4-dioxane / 18 h / 20 °C

2: benzotriazol-1-ol; triethylamine; 1,1'-carbonyldiimidazole / dichloromethane; N,N-dimethyl-formamide / 18 h / 0 - 20 °C

3: hydrogen; palladium 10% on activated carbon / methanol / 1 h / 20 °C / 760.05 Torr

4: triethylamine / dichloromethane / 5 h / 20 °C

5: hydrogenchloride / 1,4-dioxane / 1 h / 20 °C

With hydrogenchloride; palladium 10% on activated carbon; hydrogen; benzotriazol-1-ol; triethylamine; 1,1'-carbonyldiimidazole; sodium hydroxide; In 1,4-dioxane; methanol; dichloromethane; water; N,N-dimethyl-formamide;