(S)-Methyl 6-amino-2-benzamidohexanoate hydrochloride

Base Information

Chemical Name:(S)-Methyl 6-amino-2-benzamidohexanoate hydrochloride
CAS No.:14280-01-4
Molecular Formula:C14H20 N2 O3 . Cl H
Molecular Weight:300.78
Hs Code.:2924299090
European Community (EC) Number:960-789-0
Mol file:14280-01-4.mol

Synonyms:14280-01-4;BZ-LYS-OME HCL;(S)-Methyl 6-amino-2-benzamidohexanoate hydrochloride;N-alpha-Benzoyl-L-lysine methyl ester hydrochloride;Bz-L-Lys-OMe Hydrochloride;Bzo-Lys-OMe.HCl;Bz-lys-ome hydrochloride;methyl (2S)-6-amino-2-benzamidohexanoate;hydrochloride;MFCD00235873;AKOS015892640;DS-4940;Methyl benzoyl-L-lysinate hydrochloride;Benzoyl-L-lysine methyl ester hydrochloride;(s)-methyl 6-amino-2-benzamidohexanoate hcl;CS-0150967;N-Benzoyl-L-lysine methyl ester hydrochloride;F10635;L-Lysine,n2-benzoyl-,methyl ester,monohydrochloride(9ci)

Suppliers and Price of (S)-Methyl 6-amino-2-benzamidohexanoate hydrochloride

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

Usbiological
N-alpha-Benzoyl-L-lysine methyl ester hydrochloride
500mg
$ 418.00

TRC
Bz-lys-omeHydrochloride
100mg
$ 75.00

Iris Biotech GmbH
Bz-L-Lys-OMe*HCl
1 g
$ 189.00

Iris Biotech GmbH
Bz-L-Lys-OMe*HCl
5 g
$ 810.00

Crysdot
(S)-Methyl6-amino-2-benzamidohexanoatehydrochloride 97%
10g
$ 554.00

Crysdot
(S)-Methyl6-amino-2-benzamidohexanoatehydrochloride 97%
5g
$ 327.00

Chem-Impex
Nα-Benzoyl-L-lysinemethylesterhydrochloride,98%(HPLC) 98%(HPLC)
250MG
$ 46.37

Chem-Impex
Nα-Benzoyl-L-lysinemethylesterhydrochloride,98%(HPLC) 98%(HPLC)
1G
$ 123.20

Chem-Impex
Nα-Benzoyl-L-lysinemethylesterhydrochloride,98%(HPLC) 98%(HPLC)
2.5G
$ 231.84

Chemenu
(S)-Methyl6-amino-2-benzamidohexanoatehydrochloride 97%
10g
$ 524.00

Total 19 raw suppliers

Chemical Property of (S)-Methyl 6-amino-2-benzamidohexanoate hydrochloride

Chemical Property:

Vapor Pressure:6.93E-09mmHg at 25°C
Boiling Point:466.7°Cat760mmHg
Flash Point:236°C
PSA：81.42000
Density:1.118g/cm³
LogP:2.98020
Storage Temp.:Store at RT.
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:8
Exact Mass:300.1240702
Heavy Atom Count:20
Complexity:288

Purity/Quality:

97% ^*data from raw suppliers

N-alpha-Benzoyl-L-lysine methyl ester hydrochloride ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC(=O)C(CCCCN)NC(=O)C1=CC=CC=C1.Cl
Isomeric SMILES:COC(=O)[C@H](CCCCN)NC(=O)C1=CC=CC=C1.Cl

Technology Process of (S)-Methyl 6-amino-2-benzamidohexanoate hydrochloride

There total 3 articles about (S)-Methyl 6-amino-2-benzamidohexanoate hydrochloride 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:

: 331714-14-8
(S)-methyl 2-(benzoylamino)-6-(((tert-butyloxy)carbonyl)amino)hexanoate

: 14280-01-4
(2S)-N^α-benzoyllysine methyl ester hydrochloride

Guidance literature:: With hydrogenchloride; In 1,4-dioxane; dichloromethane; at 25 ℃; for 3h;
DOI:10.1021/ja003579+

Reference yield:

: 98-88-4
benzoyl chloride

: 14280-01-4
(2S)-N^α-benzoyllysine methyl ester hydrochloride

Guidance literature:: Multi-step reaction with 2 steps

1: 78 percent / i-Pr₂NEt / CH₂Cl₂ / 1 h / 25 °C

2: aq. HCl / dioxane; CH₂Cl₂ / 3 h / 25 °C

With hydrogenchloride; N-ethyl-N,N-diisopropylamine; In 1,4-dioxane; dichloromethane;
DOI:10.1021/ja003579+

Reference yield:

: 2389-48-2
N-ε-tert-butoxycarbonyl-L-lysine methyl ester hydrochloride

: 14280-01-4
(2S)-N^α-benzoyllysine methyl ester hydrochloride

Guidance literature:: Multi-step reaction with 2 steps

1: 78 percent / i-Pr₂NEt / CH₂Cl₂ / 1 h / 25 °C

2: aq. HCl / dioxane; CH₂Cl₂ / 3 h / 25 °C

With hydrogenchloride; N-ethyl-N,N-diisopropylamine; In 1,4-dioxane; dichloromethane;
DOI:10.1021/ja003579+