| Name | (2S)-2,6-bis[(2-methylpropan-2-yl)oxycarbonylamino]hexanoic acid |
|---|---|
| Synonyms |
Nα,ε-Bis-Boc-L-lysine
Nalpha,Nepsilon-Di-Boc-L-lysine di-BOC-L-lysine L-Lysine-d4-bis-N-t-BOC Boc-L-Lys(Boc)-OH MFCD00038515 N2,N6-Bis(tert-butyloxycbonyl)-L-lysine (Tert-Butoxy)carbonyl Lys(Boc)-OH(Syrup) (2S)-2,6-Bis({[(Tert-Butoxy)Carbonyl]Amino})Hexanoic Acid NA, NE-BIS-BOC-L-LYSINE Nalpha,Nsilon-Di-Boc-L-lysine Di-tert-butoxycbonyl-L-lysine (2S)-2,6-bis[(2-methylpropan-2-yl)oxycbonylamino]hexanoic acid Nα,Nε-Bis(tert-butoxycbonyl)-L-lysine Di[N-(tert-butoxycbonyl)]-L-lysine Na, Ne-Diboc-L-lysine BOC-L-LYS(BOC) N-ALPHA,SILON-BIS-BOC-L-LYSINE (2S)-2,6-bis[(2-methylpropan-2-yl)oxycbonylamino]hexanoicaci N-beta,silon-bis-Boc-L-lysine Nalpha,Nsilon-Di-Boc-L-lysine N-tert-Butoxycbonyl-Nε-Boc-L-lysine (S)-2,6-Bis-tert-butoxycarbonylaminohexanoic acid AmbotzBAA1104 N2,N6-Bis-(tert-butoxycbonyl)-L-lysine BOC-L-LYSINE(BOC) (S)-2,6-Bis((tert-butoxycarbonyl)amino)hexanoic acid N2,N6-Bis-Boc-L-lysine Nα, Nε-Bis-boc-L-lysine BOC-LYS(BOC) N-ALPHA,N-SILON-DI-T-BUTOXYCBONYL-L-LYSINE L-Lysine,N2,N6-bis[(1,1-dimethylethoxy)carbonyl] BOC-LYS(BOC)-OH NAlpha, Nsilon-Bis-boc-L-lysine N,N'-di-Boc-L-lysine Di[N-(tert-butoxycarbonyl)]-L-lysine (S)-2,6-Bis-tert-butoxycbonylaminohexanoic acid //BP Lysine Impurity 15 (Di-Boc-L-lysine) Nα,ε-Bis-Boc-L-lysine (HPLC) (S)-2,6-BIS-TERT-BUTOXYCBONYLAMINO-HEXANOIC ACID N2,N6-Bis[(1,1-dimethylethoxy)carbonyl]-L-lysine TIANFUCHEM-2-7--(S)-2,6-Bis-tert-butoxycbonylaminohexanoic acid 6-Bis-tert-butoxycbonylaminohexanoic acid N2,N6-Bis(tert-butoxycbonyl)lysine Boc-Lys(Boc)-0H Nα,Nε-Bis-Boc-L-Lys-OH N,N-Bis{[(2-methyl-2-propanyl)oxy]carbonyl}-L-lysine 2-amino-7-[(2-methylpropan-2-yl)oxy]-2-[(2-methylpropan-2-yl)oxy-oxomethyl]-7-oxohtanoic acid N,N-Bis(tert-butoxycarbonyl)-L-lysine |
| Description | (S)-2,6-Bis((tert-butoxycarbonyl)amino)hexanoic acid is a polypeptide derivative, can be used to synthesis multifunctional amphiphilic peptide dendrimer, as a nonviral gene vectors, realizes the method in cancer research. (S)-2,6-Bis((tert-butoxycarbonyl)amino)hexanoic acid also involves in the synthesis of an organic substance that increases the luminescence intensity of alkaline phosphatase substrates[1][2]. |
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| Related Catalog | |
| References |
| Density | 1.1±0.1 g/cm3 |
|---|---|
| Boiling Point | 514.4±45.0 °C at 760 mmHg |
| Molecular Formula | C16H30N2O6 |
| Molecular Weight | 346.419 |
| Flash Point | 264.9±28.7 °C |
| Exact Mass | 346.210388 |
| PSA | 113.96000 |
| LogP | 2.52 |
| Vapour Pressure | 0.0±2.9 mmHg at 25°C |
| Index of Refraction | 1.478 |
| Storage condition | Store at 0°C |
| Hazard Codes | Xn |
|---|---|
| HS Code | 2924199090 |
| Precursor 10 | |
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| DownStream 6 | |
| HS Code | 2924199090 |
|---|---|
| Summary | 2924199090. other acyclic amides (including acyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0% |