34404-36-9
34404-36-9 structure
- Name: BOC-LYS(Z)-OSU
- Chemical Name: Boc-Lys(Z)-OSu
- CAS Number: 34404-36-9
- Molecular Formula: C23H31N3O8
- Molecular Weight: 477.508
- Catalog: Research Areas Others
- Create Date: 2018-12-27 12:18:48
- Modify Date: 2026-07-03 22:27:17
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Boc-Lys(Z)-OSu is a lysine derivative[1].
| Name | Boc-Lys(Z)-OSu |
|---|---|
| Synonyms |
(S)-2,5-dioxopyrrolidin-1-yl 6-(((benzyloxy)carbonyl)amino)-2-((tert-butoxycbonyl)amino)hexanoate
EINECS 251-999-7 Nε-Z-Nα-Boc-L-lysine hydroxysuccinimide ester, Nα-Boc-Nε-Cbz-L-lysine N-hydroxysuccinimide ester, Nα-Boc-Nε-Z-L-lysine hydroxysuccinimide ester NEPSILON-Benzyloxycarbonyl-NALPHA-tert-butoxycarbonyl-L-lysine-hydroxysuccinimid N-[(N2,N6-Dicboxy-L-lysyl)oxy]succinimide N6-benzyl tert-butyl ester nα-boc-nε-cbz-l-lysine n-hydroxysuccinimide ester Nα-Boc-Nε-Z-L-lysine hydroxysuccinimide ester [5-[[(1,1-Dimethylethoxy)carbonyl]amino]-6-[(2,5-dioxo-1-pyrrolidinyl)oxy]-6-oxohexyl]cbamic acid phenylmethyl ester, (S) N-(tert-butoxycbonyl)-N-Z-L-lysine hydroxysuccinimide MFCD00037915 NA-BOC-NE-CBZ-L-LYSINEHYDROXYSUCCINIMIDEESTER N-(tert-butoxycarbonyl)-N-Z-L-lysine hydroxysuccinimide Boc-L-Lys(Cbz)-OSu 2,5-dioxopyrrolidin-1-yl (S)-6-[(benzyloxycarbonyl)amino]-2-[(tert-butoxycarbonyl)amino]hexanoate Boc-Lys(Z)-Osu Boc-L-Lys(Z)-OSu benzyl (S)-[5-[[(1,1-dimethylethoxy)carbonyl]amino]-6-[(2,5-dioxo-1-pyrrolidinyl)oxy]-6-oxohexyl]cbamate (Tert-Butoxy)carbonyl Lys(Z)-OSu benzyl N-[(5S)-5-{[(tert-butoxy)carbonyl]amino}-6-(2,5-dioxopyrrolidin-1-yl)-6-oxohexyl]cbamate Nα-Boc-Nε-Z-L-lysine N-hydroxysuccinimide ester L-Lysine,N2-[(1,1-dimethylethoxy)carbonyl]-N6-[(phenylmethoxy)carbonyl]-,2,5-dioxo-1-pyrrolidinyl ester 2,5-Dioxopyrrolidin-1-yl N-[(benzyloxy)carbonyl]-N-(tert-butoxycarbonyl)-L-lysinate Boc-Lys-(CBz)-succinimide ester N2-[(1,1-Dimethylethoxy)carbonyl]-N6-[(phenylmethoxy)carbonyl]-L-lysine 2,5-dioxo-1-pyrrolidinyl ester N-alpha-Boc-Nsilon-Z-L-lysine N-hydroxysuccinimide ester Boc-Lys(Z)-Osuc 2,5-Dioxo-1-pyrrolidinyl N-[(benzyloxy)carbonyl]-N-{[(2-methyl-2-propanyl)oxy]carbonyl}lysinate Boc-Lys(Ne-Cbz)-ONSu [(S)-5-[[(1,1-Dimethylethoxy)carbonyl]amino]-6-[(2,5-dioxo-1-pyrrolidinyl)oxy]-6-oxohexyl]cbamic acid phenylmethyl ester Nsilon-Benzyloxycbonyl-Nalpha-Boc-L-lysine N-succinimidyl ester (2,5-dioxopyrrolidin-1-yl) (2S)-2-[(2-methylpropan-2-yl)oxycbonylamino]-6-(phenylmethoxycbonylamino)hexanoate Lysine, N-[(1,1-dimethylethoxy)carbonyl]-N-[(phenylmethoxy)carbonyl]-, 2,5-dioxo-1-pyrrolidinyl ester Benzyl (S)-(5-(((1,1-dimethylethoxy)carbonyl)amino)-6-((2,5-dioxo-1-pyrrolidinyl)oxy)-6-oxohexyl)carbamate NA-T-BOC-N-SILON-CBZ-L-LYSINE N-HYDROX YSUCCINIMI N^e-Benzyloxycbonyl-N^a-Boc-L-lysine N-hydroxysucciniMide ester N-[(N2,N6-Dicarboxy-L-lysyl)oxy]succinimide N6-benzyl tert-butyl ester [(5S)-5-[[(1,1-Dimethylethoxy)carbonyl]amino]-6-[(2,5-dioxo-1-pyrrolidinyl)oxy]-6-oxohexyl] cbamic acid phenylmethyl ester L-Lysine, N-[(1,1-dimethylethoxy)carbonyl]-N-[(phenylmethoxy)carbonyl]-, 2,5-dioxo-1-pyrrolidinyl ester NSILON-Benzyloxycbonyl-NALPHA-tert-butoxycbonyl-L-lysine-hydroxysuccinimid Nalpha-(tert-Butyloxycbonyl)-Nε-(benzyloxycbonyl)-L-lysine N-hydroxysuccinimide ester Boc-Lyz(Z)-OSu Nα-Boc-Nε-Z-L-lysineN-hydroxysuccinimide ester (HPLC) Nε-Z-Nα-Boc-L-lysine hydroxysuccinimide ester |
| Description | Boc-Lys(Z)-OSu 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 | 1.3±0.1 g/cm3 |
|---|---|
| Melting Point | 108-115ºC |
| Molecular Formula | C23H31N3O8 |
| Molecular Weight | 477.508 |
| Exact Mass | 477.211121 |
| PSA | 140.34000 |
| LogP | 1.62 |
| Index of Refraction | 1.557 |
| Storage condition | -20°C |
| Hazard Codes | Xi |
|---|---|
| RIDADR | NONH for all modes of transport |
| WGK Germany | 3 |
|
~83%
34404-36-9 |
| Literature: Jaoudai, Mahmoud; Martinez, Jean; Castro, Bertrand Journal of Organic Chemistry, 1987 , vol. 52, # 12 p. 2364 - 2367 |
|
~99%
34404-36-9 |
| Literature: Rosowsky, Andre; Wright, Joel E. Journal of Organic Chemistry, 1989 , vol. 54, # 23 p. 5551 - 5558 |
| Precursor 3 | |
|---|---|
| DownStream 0 | |