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Product Name: (S)-2-((((9H-FLUOREN-9-YL)METHOXY)CARBONYL)AMINO)-6-(((4-METHOXYPHENYL)DIPHENYLMETHYL)AMINO)HEXANOIC ACID
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159857-60-0

159857-60-0 structure

159857-60-0 structure

Name: Fmoc-Lys(MMt)-OH
Chemical Name: (2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-6-[[(4-methoxyphenyl)-diphenylmethyl]amino]hexanoic acid
CAS Number: 159857-60-0
Molecular Formula: C₄₁H₄₀N₂O₅
Molecular Weight: 640.767
Catalog: Research Areas Others
Create Date: 2019-01-01 12:06:16
Modify Date: 2026-07-07 13:51:28
N2-(((9H-Fluoren-9-yl)methoxy)carbonyl)-N6-((4-methoxyphenyl)diphenylmethyl)-L-lysine is a lysine derivative[1].

Name	(2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-6-[[(4-methoxyphenyl)-diphenylmethyl]amino]hexanoic acid
Synonyms	Fmoc-Lys(Mmt)-OH FMOC-LYS(MMT)-OH N6-[Diphenyl(4-methoxyphenyl)methyl]-N2-{[(9H-fluoren-9-yl)methoxy]carbonyl}-L-lysine, FMOC-L-LYS(MMT)-OH N6-(4-Methoxytrityl)-L-lysine N2-FMOC protected Fmoc-Lys(MMT) N-alpha-Fmoc-Nε-4-methoxyyltrityl-L-lysine (S)-2-((((9H-Fluo L-Lysine, N2-[(9H-fluoren-9-ylmethoxy)carbonyl]-N6-[(4-methoxyphenyl)diphenylmethyl] Fmoc-Lys-OH Novabiochem (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-6-(((4-Methoxyphenyl)diphenylmethyl)amino)he Nα-Fmoc-Nε-4-methoxyyltrityl-L-lysine (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-6-(((4-Methoxyphenyl)diphenylmethyl)amino)hexan N6-[Diphenyl(4-methoxyphenyl)methyl]-N2-{[(9H-fluoren-9-yl)methoxy]carbonyl}-L-lysine N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-N'-[(4-methoxyphenyl)diphenylmethyl]-L-lysine N-alpha-Fmoc-N-silon-4-methoxytrity Fmoc-L-lysine(methoxytrityl)-OH AmbotzFAA1622 (2S)-2-(9H-fluoren-9-ylmethoxycbonylamino)-6-[[(4-methoxyphenyl)-diphenylmethyl]amino]hexanoicaci (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-6-(((4-Methoxyphenyl)diphenylmethyl)amino)hexanoic acid (9H-Fluoren-9-yl)MethOxy]carbonyl Lys(MMt)-OH N2-(((9H-Fluoren-9-yl)methoxy)carbonyl)-N6-((4-methoxyphenyl)diphenylmethyl)-L-lysine Nα-Fmoc-Nε-4-methoxyyltrityl-L-lysine (HPLC, Chiral purity) N-Fmoc-N'-[(4-methoxyphenyl)methyldiphenyl]-L-lysine Nα-Fmoc-Nsilon-4-methoxyyltrityl-L-lysine N6-(4-Methoxytrityl)-L-lysine, N2-FMOC protected N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-N-[(4-methoxyphenyl)(diphenyl)methyl]-L-lysine (S)-2-(((9H-fluoren-9-yl)methyl9H-fluoren-9-yl)methoxy)cbonylamino)-6-((4-methoxyphenyl)diphenylmethylamino)hexanoic acid Fmoc-L-Lys(Mmt)-OH Fmoc-Lys(mTrt)-OH (2S)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-6-{[(4-methoxyphenyl)diphenylmethyl]amino}hexanoic acid Fmoc-Lys(Mtt)-OH

Description	N2-(((9H-Fluoren-9-yl)methoxy)carbonyl)-N6-((4-methoxyphenyl)diphenylmethyl)-L-lysine is a lysine derivative[1].
Related Catalog	Research Areas >> Others Signaling Pathways >> Others >> Others
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	[1]. Luckose F, et al. Effects of amino acid derivatives on physical, mental, and physiological activities. Crit Rev Food Sci Nutr. 2015;55(13):1793-1144.

Density	1.2±0.1 g/cm3
Boiling Point	814.1±65.0 °C at 760 mmHg
Molecular Formula	C₄₁H₄₀N₂O₅
Molecular Weight	640.767
Flash Point	446.2±34.3 °C
Exact Mass	640.293701
PSA	96.89000
LogP	9.23
Vapour Pressure	0.0±3.1 mmHg at 25°C
Index of Refraction	1.619
Storage condition	2-8°C

105047-45-8 structure

105047-45-8

14470-28-1 structure

14470-28-1

~%

159857-60-0 structure

159857-60-0

Literature: Weinshenker, Ned M.; West, Frederick G.; Araneo, Barbara A.; Li, Weiping Patent: US2005/54607 A1, 2005 ; Location in patent: Page/Page column 17 ;

Precursor 2
105047-45-8 14470-28-1
DownStream 0

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