| Name | N6-Cbz-L-lysine Benzyl Ester Hydrochloride |
|---|---|
| Synonyms |
(S)-Benzyl 2-amino-6-(((benzyloxy)carbonyl)amino)hexanoate hydrochloride
N^e-Benzyloxycbonyl-L-lysine benzyl ester hydrochloride N6-Cbobenzoxy-L-lysine Benzyl Ester Hydrochloride benzyl N6-benzyloxycbonyl-L-lysinate hydrochloride H-Lys(Cbz)-OBzl·Hydrochloride n(sup6)-(phenylacetoxy)-,benzylester,monohydrochloride,l-lysin N6-Cbz-L-Lysine benzyl ester HCl H-Lys(Z)-OBzl·HCl Benzyl N-[(benzyloxy)carbonyl]-L-lysinate hydrochloride (1:1) N6-Cbz-L-Lysine benzyl ester hydrochloride //BP N-Benzyloxycbonyl-L-lysine benzyl ester hydrochloride LYS(Z)-OBZLCL 2-amino-6-(phenylmethoxycbonylamino)hexanoic acid (phenylmethyl) ester hydrochloride benzyl (2S)-2-amino-6-{[(benzyloxy)carbonyl]amino}hexanoate hydrochloride H-L-Lys(Z)-OBzl*HCl Nε-Z-L-lysine benzyl ester hydrochloride N-ε-Z-L-lysine benzyl ester hydrochloride N6-Cbz-L-Lysine benz EINECS 228-859-9 Nε-Cbobenzyloxy-L-lysine benzyl ester hydrochloride L-Lys(Cbz)-OBzl HCl H-LYS(CBZ)-OBZL·HCL n(6)-cboxy-,dibenzylester,hydrochloride,l-lysin N6-[(PhenylMethoxy)carbonyl]-L-lysine PhenylMethyl Ester Hydrochloride L-Lysine, N-[(phenylmethoxy)carbonyl]-, phenylmethyl ester, hydrochloride (1:1) MFCD00038981 N6-Cbobenzyloxy-L-lysine Benzyl Ester Hydrochloride H-Lys(Z)-OBzl·HCI N-SILON-CBZ-L-LYSINE BENZYL ESTERHYDRO CHLORIDE C Lys(Z)-OBzl·HCl L-LYS(Z)-OBZL.HCL n-e-z-l-lysinebenzylesterhydrochloride Nε-Z-L-lysine benzyl ester hydrochloride (HPLC) H-LYS(Z)-OBZL.HCL n-silon-cbobenzyloxy-l-lysinebenzylesterhydrochloride N-SILON-BENZYLOXYCBONYL-L-LYSINE BENZYL ESTER HYDROCHLORIDE Nε-Cbz-L-Lysine benzyl ester hydrochloride l-lysine,n(6)-((phenylmethoxy)carbonyl)-,phenylmethylester,monohydrochlor N6-Carbobenzyloxy-L-lysine Benzyl Ester Hydrochloride |
| Description | N6-Carbobenzoxy-L-lysine benzyl ester hydrochloride is a lysine derivative[1]. |
|---|---|
| Related Catalog | |
| In Vitro | Amino acids and amino acid derivatives have been commercially used as ergogenic supplements. They influence the secretion of anabolic hormones, supply of fuel during exercise, mental performance during stress related tasks and prevent exercise induced muscle damage. They are recognized to be beneficial as ergogenic dietary substances[1]. |
| References |
| Density | 1.163g/cm3 |
|---|---|
| Boiling Point | 511.7ºC at 760 mmHg |
| Melting Point | 138-140ºC |
| Molecular Formula | C21H27ClN2O4 |
| Molecular Weight | 406.903 |
| Flash Point | 263.2ºC |
| Exact Mass | 406.165924 |
| PSA | 90.65000 |
| LogP | 5.04700 |
| Index of Refraction | 1.562 |
| Storage condition | Store at RT. |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
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| Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
|---|---|
| Hazard Codes | Xi |
| RIDADR | NONH for all modes of transport |
| WGK Germany | 3 |
| RTECS | OL5685000 |
| HS Code | 2924299090 |
|
~93%
6366-70-7 |
| Literature: Kulikov, S. V.; Leonova, E. B.; Kalinina, N. M.; Samartsev, M. A.; Bubnova, L. N.; et al. Russian Journal of Bioorganic Chemistry, 1995 , vol. 21, # 6 p. 362 - 369 Bioorganicheskaya Khimiya, 1995 , vol. 21, # 6 p. 421 - 429 |
|
~%
6366-70-7 |
| Literature: US1312 H1, ; |
|
~%
6366-70-7 |
| Literature: Journal of Medicinal Chemistry, , vol. 48, # 13 p. 4285 - 4292 |
|
~%
6366-70-7 |
| Literature: Bioorganic and Medicinal Chemistry, , vol. 18, # 17 p. 6220 - 6229 |
|
~%
6366-70-7 |
| Literature: Journal of Medicinal Chemistry, , vol. 48, # 13 p. 4285 - 4292 |
| Precursor 5 | |
|---|---|
| DownStream 2 | |
| HS Code | 2924299090 |
|---|---|
| Summary | 2924299090. other cyclic amides (including cyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0% |