139262-23-0
- Product Name：Nalpha-Fmoc-L-lysine hydrochloride
- Molecular Formula：C21H25ClN2O4
- Purity：99%
- Molecular Weight：404.894
Product Details;
CAS#： 139262-23-0
Molecular Formula： C21H25ClN2O4
Factory Supply Top Purity 139262-23-0 Customized Supply
- Molecular Formula:C21H24N2O4*ClH
- Molecular Weight:404.894
- Vapor Pressure:1.29E-15mmHg at 25°C
- Refractive Index:-11.0 ° (C=1, DMF)
- Boiling Point:607.6 °C at 760 mmHg
- Flash Point:321.3 °C
- PSA：101.65000
- LogP:5.00050
Nalpha-Fmoc-L-lysine hydrochloride(Cas 139262-23-0) Usage
InChI:InChI=1/C21H24N2O4.ClH/c22-12-6-5-11-19(20(24)25)23-21(26)27-13-18-16-9-3-1-7-14(16)15-8-2-4-10-17(15)18;/h1-4,7-10,18-19H,5-6,11-13,22H2,(H,23,26)(H,24,25);1H/t19-;/m0./s1
139262-23-0 Relevant articles
Investigating d-lysine stereochemistry for epigenetic methylation, demethylation and recognition
Belle, Roman,Al Temimi, Abbas H. K.,Kumar, Kiran,Pieters, Bas J. G. E.,Tumber, Anthony,Dunford, James E.,Johansson, Catrine,Oppermann, Udo,Brown, Tom,Schofield, Christopher J.,Hopkinson, Richard J.,Paton, Robert S.,Kawamura, Akane,Mecinovi?, Jasmin
supporting information, p. 13264 - 13267 (2017/12/26)
Histone lysine methylation is regulated ...
139262-23-0 Process route
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- 92122-45-7
Fmoc-D-Lys(BOC)-OH
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- 201002-47-3,139262-23-0
Fmoc-Lys-OH hydrochloride
| Conditions | Yield |
|---|---|
|
With hydrogenchloride; In diethyl ether; dichloromethane; for 16h;
|
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- 139262-23-0
9-fluorenylmethoxycarbonyl-L-alanine hydrochloride
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- 951695-85-5,2044709-77-3
Νε-tert-butoxycarbonyl-Να-(9-fluorenylmethoxycarbonyl)-Νε-methyllysine
| Conditions | Yield |
|---|---|
|
Multi-step reaction with 4 steps
1: N-ethyl-N,N-diisopropylamine / methanol; tetrahydrofuran / 9 h / 0 - 20 °C
2: sodium cyanoborohydride / water; methanol / 10 h / 20 °C
3: hydrogenchloride / water; methanol / 1 h / 20 °C / pH 5 - 6
4: sodium hydrogencarbonate / water; tetrahydrofuran / 4 h / 20 °C
With hydrogenchloride; sodium cyanoborohydride; sodium hydrogencarbonate; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; methanol; water;
|
|
|
Multi-step reaction with 4 steps
1: N-ethyl-N,N-diisopropylamine / methanol; tetrahydrofuran / 9 h / 0 - 20 °C
2: sodium tetrahydroborate / water; methanol / 8 h / 20 °C
3: hydrogenchloride / water; methanol / 1 h / 20 °C / pH 5 - 6
4: sodium hydrogencarbonate / water; tetrahydrofuran / 4 h / 20 °C
With hydrogenchloride; sodium tetrahydroborate; sodium hydrogencarbonate; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; methanol; water;
|
|
|
Multi-step reaction with 4 steps
1: N-ethyl-N,N-diisopropylamine / methanol; tetrahydrofuran / 9 h / 0 - 20 °C
2: sodium cyanoborohydride / water; methanol / 8 h / 20 °C
3: hydrogenchloride / water; methanol / 1 h / 20 °C / pH 5 - 6
4: sodium hydrogencarbonate / water; tetrahydrofuran / 4 h / 20 °C
With hydrogenchloride; sodium cyanoborohydride; sodium hydrogencarbonate; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; methanol; water;
|
139262-23-0 Upstream products
-
92122-45-7
Fmoc-D-Lys(BOC)-OH
139262-23-0 Downstream products
-
88125-05-7
Nε-(1-deoxy-fructos-1-yl)-L-lysine
-
158478-81-0
(S)-11-((tert-butoxycarbonyl)amino)-1-(9H-fluoren-9-yl)-15,15-dimethyl-3,13-dioxa-2,14-dioxa-4,10,12-triazahexadecyl-11-ene-5-carboxylic acid
-
1334231-01-4
(S)-2-((S)-2-((R)-2-amino-3-phenylpropanamido)-6-(ethanethioamido)hexanamido)propanoic acid
-
1334231-03-6
(S)-2-((S)-6-(ethanethioamido)-2-(3-phenylpropanamido)hexanamido)propanoic acid
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