Nε-(Ethoxycarbonylethyl)-L-lysine Methyl Ester (Mixture of Diastereomers)

Base Information

Chemical Name:Nε-(Ethoxycarbonylethyl)-L-lysine Methyl Ester (Mixture of Diastereomers)
CAS No.:103954-36-5
Molecular Formula:C12H24N2O4
Molecular Weight:260.33
Hs Code.:

Synonyms:Nε-(Ethoxycarbonylethyl)-L-lysine Methyl Ester (Mixture of Diastereomers);(S)-N6-(2-Ethoxy-1-Methyl-2-oxoethyl)-L-lysine Methyl Ester

Suppliers and Price of Nε-(Ethoxycarbonylethyl)-L-lysine Methyl Ester (Mixture of Diastereomers)

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

TRC
Nε-(Ethoxycarbonylethyl)-L-lysineMethylEster(MixtureofDiastereomers)
500mg
$ 1230.00

TRC
Nε-(Ethoxycarbonylethyl)-L-lysineMethylEster(MixtureofDiastereomers)
50mg
$ 155.00

Total 2 raw suppliers

Chemical Property of Nε-(Ethoxycarbonylethyl)-L-lysine Methyl Ester (Mixture of Diastereomers)

Chemical Property:

PSA：90.65000
LogP:1.28940
Solubility.:Chloroform, Dichloromethane, Ether, Methanol

Purity/Quality:

99% ^*data from raw suppliers

Nε-(Ethoxycarbonylethyl)-L-lysineMethylEster(MixtureofDiastereomers) ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Uses Lysine derivative.

Technology Process of Nε-(Ethoxycarbonylethyl)-L-lysine Methyl Ester (Mixture of Diastereomers)

There total 8 articles about Nε-(Ethoxycarbonylethyl)-L-lysine Methyl Ester (Mixture of Diastereomers) 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: 89.0%

: 687-64-9
L-lysine methyl ester

: 84028-88-6
ethyl (S)-lactate triflate

: 103954-34-3,103954-35-4,103954-36-5
(2S,1'R)-N⁶-<1-(Ethoxycarbonyl)ethyl>lysin-methylester

Guidance literature:: In dichloromethane; at 20 ℃; for 4h;

Reference yield: 81.0%

: 103954-29-6,103954-30-9
(2S,1'R)-N²-(Benzyloxycarbonyl)-N⁶-<1-(ethoxycarbonyl)ethyl>lysin-methylester

: 103954-34-3,103954-35-4,103954-36-5
(2S,1'R)-N⁶-<1-(Ethoxycarbonyl)ethyl>lysin-methylester

Guidance literature:: With hydrogen; palladium on activated charcoal; In tetrahydrofuran; water; acetic acid; at 20 ℃; under 735.5 Torr;

Reference yield:

: 5591-93-5
(S)-methyl 6-amino-2-(benzyloxycarbonylamino)hexanoate

: 103954-34-3,103954-35-4,103954-36-5
(2S,1'R)-N⁶-<1-(Ethoxycarbonyl)ethyl>lysin-methylester

Guidance literature:: Multi-step reaction with 2 steps

1: 94 percent / K₂CO₃ / CH₂Cl₂ / 6 h / 20 °C

2: 81 percent / H₂ / 30percent Pd/C / tetrahydrofuran; H₂O; acetic acid / 20 °C / 735.5 Torr

With hydrogen; potassium carbonate; palladium on activated charcoal; In tetrahydrofuran; dichloromethane; water; acetic acid;