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FMoc-α-Me-Lys(Boc)-OH

FMoc-α-Me-Lys(Boc)-OH Structure
CAS No.
1202003-49-3
Chemical Name:
FMoc-α-Me-Lys(Boc)-OH
Synonyms
(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-6-((tert-butoxycarbonyl)amino)-2-methylhexanoic acid;Fmoc-a-Me-Lys(Boc)-OH;Fmoc-α-Me-Lys(Boc)-OH;Fmoc-alpha-Me-Lys(Boc)-OH;Fmoc-α-methyl-L-Lysine(Boc);Fmoc-alpha-Me-L-Lys(Boc)-OH;FMoc-α-Me-Lys(Boc)-OH USP/EP/BP;N6-Boc-N2-Fmoc-alfa-Me--L-Lys-OH;N6-Boc-N2-Fmoc-2-methyl-L-Lysine;(S)-Na-Fmoc-NW-Boc-α-Methyllysine
CBNumber:
CB82729321
Molecular Formula:
C27H34N2O6
Molecular Weight:
482.57
MOL File:
1202003-49-3.mol
Modify Date:
2023/4/27 16:27:43

FMoc-α-Me-Lys(Boc)-OH Properties

Boiling point 687.9±55.0 °C(Predicted)
Density 1.196±0.06 g/cm3(Predicted)
storage temp. 2-8°C
pka 3.92±0.41(Predicted)
form powder
color white
InChIKey MYQXEVZHWDILHG-MHZLTWQESA-N
SMILES C(O)(=O)[C@](C)(CCCCNC(OC(C)(C)C)=O)NC(OCC1C2=C(C=CC=C2)C2=C1C=CC=C2)=O

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335-H336-H351-H373
Precautionary statements  P261-P281-P305+P351+P338
Hazard Codes  Xn
Risk Statements  36/37/38-40-67
Safety Statements  23-24/25-36/37
TSCA  No

FMoc-α-Me-Lys(Boc)-OH Chemical Properties,Uses,Production

Chemical Properties

White to off-white powder.

Synthesis

Benzyl (2R,3S)-(?)-6-oxo-2,3-diphenyl-4-morpholinecarboxylate (4) was successively alkylated with methyl iodide and 1,4-diiodobutane using a base. In each alkylation step anti-alkylated product formed exclusively. The iodo group was displaced with azide, which served as a precursor for the side-chain amino function. Catalytic hydrogenation with concomitant cleavage of the chiral auxiliary afforded (L)-α-Me-Lys-OH (9) in a total of four steps in good yield. (L)-Fmoc-α-Me-Lys(Boc)-OH (16) was obtained from 9 via regioselective benzyloxycarbonylation. Alternately, (L)-Fmoc-α-Me-Lys(Boc)-OH (16) was obtained via Staudinger reduction of azide (8) in a total of six steps in good yield.

FMoc-α-Me-Lys(Boc)-OH Suppliers

Global( 97)Suppliers
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A.J Chemicals 91-9810153283 New Delhi, India 6124 58 Inquiry
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BOC Sciences 16314854226; +16314854226 United States 19743 58 Inquiry
N6-[(1,1-Dimethylethoxy)carbonyl]-N2-[(9H-fluoren-9-ylmethoxy)carbonyl]-2-methyl-L-lysine (S)-N-ALPHA-FMOC-N-EPSILON-BOC-ALPHA-METHYLLYSINE (S)-NΑ-FMOC-NΩ-BOC-Α-METHYLLYSINE (S)-Na-Fmoc-NW-Boc-α-Methyllysine Fmoc-alpha-Me-L-Lys(Boc)-OH (2S)-6-{[(tert-butoxy)carbonyl]amino}-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-2-methylhexanoic acid (9H-Fluoren-9-yl)MethOxy]Carbonyl Alpha-Methyl-Lys(Boc)-OH N6-Boc-N2-Fmoc-alfa-Me--L-Lys-OH (S)-N-ALPHA-FMOC-N-EPSILON-BOC-ALPHA-METHYLLYSINE, >97% Fmoc-a-Me-Lys(Boc)-OH Fmoc-α-methyl-L-Lysine(Boc) (S)-Na-Fmoc-Nw-Boc-A-Methyllysine Fmoc-alpha-Me-Lys(Boc)-OH L-Lysine, N6-[(1,1-dimethylethoxy)carbonyl]-N2-[(9H-fluoren-9-ylmethoxy)carbonyl]-2-methyl- N6-Boc-N2-Fmoc-2-methyl-L-Lysine Fmoc-α-Me-Lys(Boc)-OH FMoc-α-Me-Lys(Boc)-OH USP/EP/BP N-α-(9-Fluorenylmethoxycarbonyl)-N-ε-(t-butoxycarbonyl)-α-methyl-L-lysine (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-6-((tert-butoxycarbonyl)amino)-2-methylhexanoic acid (S)-Na-Fmoc-NW-Boc-α-Methyllysine 1202003-49-3 1202003-41-3 α-Methyl Amino Acids