| Identification | Back Directory | [Name]
BOC-LYS(ME)2-OH | [CAS]
65671-53-6 | [Synonyms]
Boc-Lys(Me)
Boc-Lys(Me)-OH
BOC-LYS(ME)2-OH
Boc-L-Lys(Me)2-OH
BOC-LYSINE(ME)2-OH
Boc-N-ε-dimethyl-L-lysine
BOC-LYS(ME)2-OH USP/EP/BP
Boc-Ne,e-dimethyl-L-lysine
Nα-Boc-Nε-dimethyl-L-lysine
Boc-Lys(Me)-OH Novabiochem
N2-Boc-N6,N6-dimethyl-L-lysine
N-α-butoxycarbonyl-N-ε-L-lysine
BOC-N-EPSILON-DIMETHYL-L-LYSINE
Nα-Boc-Nε-dimethyl-L-lysine98+%
Nalpha-Boc-Nepsilon-dimethyl-L-lysine
N-ALPHA-T-BOC-N-EPSILON-DIMETHYL-L-LYSINE
N(^a)-Boc-N(^e),N(^e)-diMethyl-L-lysine, 97%
N2-(tert-Butoxycarbonyl)-N6,N6-dimethyl-L-lysine
N-[(tert-Butoxy)carbonyl]-N',N'-dimethyl-L-lysine
Na-Boc-(S)-2-amino-6-(dimethylamino)hexanoic acid
N(alpha)-Boc-N(epsilon),N(epsilon)-dimethyl-L-lysine
N-ALPHA-BOC-(S)-2-AMINO-6-(DIMETHYLAMINO)HEXANOIC ACID
L-Lysine,N2-[(1,1-dimethylethoxy)carbonyl]-N6,N6-dimethyl-
N-ALPHA-T-BUTOXYCARBONYL-N-EPSILON,N-EPSILON-DIMETHYL-L-LYSINE
(S)-2-(tert-Butoxycarbonylamino)-6-(dimethylamino)hexanoic acid
(2S)-2-{[(tert-butoxy)carbonyl]amino}-6-(dimethylamino)hexanoic acid
(2S)-6-(dimethylamino)-2-[(2-methylpropan-2-yl)oxycarbonylamino]hexanoicaci
(2S)-6-(dimethylamino)-2-[(2-methylpropan-2-yl)oxycarbonylamino]hexanoic acid | [Molecular Formula]
C13H26N2O4 | [MDL Number]
MFCD00076965 | [MOL File]
65671-53-6.mol | [Molecular Weight]
274.36 |
| Chemical Properties | Back Directory | [Boiling point ]
413.3±40.0 °C(Predicted) | [density ]
1.064±0.06 g/cm3(Predicted) | [storage temp. ]
-15°C | [form ]
powder | [pka]
3.92±0.21(Predicted) | [Major Application]
peptide synthesis | [InChI]
1S/C13H26N2O4/c1-13(2,3)19-12(18)14-10(11(16)17)8-6-7-9-15(4)5/h10H,6-9H2,1-5H3,(H,14,18)(H,16,17)/t10-/m0/s1 | [InChIKey]
KPXRFYHPDPDJSY-JTQLQIEISA-N | [SMILES]
[N+H](CCCC[C@H](NC(=O)OC(C)(C)C)C(=O)[O-])(C)C |
| Safety Data | Back Directory | [WGK Germany ]
WGK 2 water endangering | [HS Code ]
2924 19 00 | [HazardClass ]
IRRITANT | [Storage Class]
11 - Combustible Solids |
| Hazard Information | Back Directory | [Uses]
Boc-Lys(Me)2-OH is used in the synthesis of peptidyl α-keto thiazoles as tissue factor VIIa inhibitors. It is also used to prepare tetrahydropyranylglycine sulfonamides as bradykinin hB2 receptor antagonists. | [reaction suitability]
reaction type: Boc solid-phase peptide synthesis |
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| Company Name: |
Alfa Aesar
|
| Tel: |
400-6106006 |
| Website: |
http://chemicals.thermofisher.cn |
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