N2-[2-[(1-Carboxyethyl)amino]ethyl]-N6-(3-carboxy-3-hydroxy-1-oxopropyl)-L-lysine

Base Information

Chemical Name:N2-[2-[(1-Carboxyethyl)amino]ethyl]-N6-(3-carboxy-3-hydroxy-1-oxopropyl)-L-lysine
CAS No.:92308-51-5
Molecular Formula:C15H27N3O8
Molecular Weight:377.395
Hs Code.:
Mol file:92308-51-5.mol

Synonyms:2-[2-(1-Carboxy-ethylamino)-ethylamino]-6-(3-carboxy-3-hydroxy-propionylamino)-hexanoic acid;N2-{2-[(1-carboxyethyl)amino]ethyl}-N6-(3-carboxy-3-hydroxy-1-oxopropyl)lysine (rhizobactin);

Suppliers and Price of N2-[2-[(1-Carboxyethyl)amino]ethyl]-N6-(3-carboxy-3-hydroxy-1-oxopropyl)-L-lysine

Supply Marketing:

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

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Chemical Property of N2-[2-[(1-Carboxyethyl)amino]ethyl]-N6-(3-carboxy-3-hydroxy-1-oxopropyl)-L-lysine

Chemical Property:

PSA：185.29000
LogP:-0.61330

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

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Technology Process of N2-[2-[(1-Carboxyethyl)amino]ethyl]-N6-(3-carboxy-3-hydroxy-1-oxopropyl)-L-lysine

There total 11 articles about N2-[2-[(1-Carboxyethyl)amino]ethyl]-N6-(3-carboxy-3-hydroxy-1-oxopropyl)-L-lysine 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:

: 55757-60-3
N-α-(tert-butoxycarbonyl)-L-lysine methyl ester

: 92308-51-5
rhizobactin

Guidance literature:: Multi-step reaction with 6 steps

1: pyridine

2: 20percent CF₃COOH / CH₂Cl₂

3: HCl / methanol

4: NaBH₃CN / methanol

5: KOD / D₂O

6: H₂, pyridine, CH₃COOH / Pd-C / methanol / pH 5.8

With pyridine; hydrogenchloride; potassium deuteroxide; hydrogen; sodium cyanoborohydride; acetic acid; trifluoroacetic acid; palladium on activated charcoal; In methanol; dichloromethane; water-d2;
DOI:10.1016/S0040-4039(00)95188-8

Reference yield:

: (S)-2-{2-[Benzyloxycarbonyl-((R)-1-carboxy-ethyl)-amino]-ethylamino}-6-((S)-3-carboxy-3-hydroxy-propionylamino)-hexanoic acid

: 92308-51-5
rhizobactin

Guidance literature:: With pyridine; hydrogen; acetic acid; palladium on activated charcoal; In methanol; pH 5.8;
DOI:10.1016/S0040-4039(00)95188-8

Reference yield:

: 2389-45-9
Boc-Lys(Z)-OH

: 92308-51-5
rhizobactin

Guidance literature:: Multi-step reaction with 8 steps

1: diethyl ether

2: H₂ / Pd-C / methanol

3: pyridine

4: 20percent CF₃COOH / CH₂Cl₂

5: HCl / methanol

6: NaBH₃CN / methanol

7: KOD / D₂O

8: H₂, pyridine, CH₃COOH / Pd-C / methanol / pH 5.8

With pyridine; hydrogenchloride; potassium deuteroxide; hydrogen; sodium cyanoborohydride; acetic acid; trifluoroacetic acid; palladium on activated charcoal; In methanol; diethyl ether; dichloromethane; water-d2;
DOI:10.1016/S0040-4039(00)95188-8