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252049-10-8

252049-10-8 Structure

252049-10-8 Structure
IdentificationBack Directory
[Name]

FMOC-LYS(ME)2-OH HCL
[CAS]

252049-10-8
[Synonyms]

FMOC-LYS(ME)2-OH HCL
FMOC-L-LYS(ME2)-OH HCL
FMOC-LYSINE(ME)2-OH HCL
FMOC-LYS(ME)2-OH HCL 1 G
FMOC-LYS(ME)2-OH HCL USP/EP/BP
Fmoc-Lys(Me)2-OH hydrochloride
N2-Fmoc-N6,N6-dimethyl-L-lysine HCl
FMoc-Lys(Me2)-OH hydrochloride salt
Fmoc-Nε-dimethyl-L-lysine hydrochloride
Fmoc-Lys(Me2)-OHhydrochloridesalt, >97%
Fmoc-N',N'-dimethyl-L-lysine hydrochloride
FMOC-N-EPSILON-DIMETHYL-L-LYSINE HYDROCHLORIDE
(S)-N-FMoc-N',N”-diMethyl-L-lysine Hydrochloride
(S)-N-FMoc-N6,N6-diMethyl-L-lysine Hydrochloride
(9H-Fluoren-9-yl)MethOxy]Carbonyl Lys(Me)2-OH·HCl
FMoc-Nε-diMethyl-L-lysine hydrochloride
Fmoc-Nε-dimethyl-L-lysine hydrochloride≥ 98% (HPLC)
FMOC-N-EPSILON,EPSILON-DIMETHYL-L-LYSINE HYDROCHLORIDE SALT
N-ALPHA-FMOC-N-EPSILON,EPSILON-DIMETHYL-L-LYSINE HYDROCHLORIDE SALT
N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-N',N'-dimethyl-L-lysine hydrochloride
N2-[(9H-Fluoren-9-ylMethoxy)carbonyl]-N6,N6-diMethyl-L-Lysine Hydrochloride
(S)-2-(((9H-fluoren-9-yl)methoxy)carbonylamino)-6-(dimethylamino)hexanoic acid
N-ALPHA-(9-FLUORENYLMETHYLOXYCARBONYL)-N-EPSILON-DIMETHYL-L-LYSINE HYDROCHLORIDE
N2-[(9H-Fluoren-9-ylmethoxy)carbonyl]-N6,N6-dimethyl-L-lysine hydrochloride (1:1)
L-Lysine, N2-[(9H-fluoren-9-ylmethoxy)carbonyl]-N6,N6-dimethyl-, hydrochloride (1:1)
N-ALPHA-(9-FLUORENYLMETHOXYCARBONYL)-N-EPSILON,N-EPSILON-DIMETHYL-L-LYSINE HYDROCHLORIDE
(S)-2-((((9H-Fluoren-9-yl)Methoxy)carbonyl)aMino)-6-(diMethylaMino)hexanoic acid hydrochloride
(2S)-6-(dimethylamino)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)hexanoic acid hydrochloride
(S)-2-(((9H-fluoren-9-yl)methyl9H-fluoren-9-yl)methoxy)carbonylamino)-6-(dimethylamino)hexanoic acid hydrochloride
[Molecular Formula]

C23H29ClN2O4
[MDL Number]

MFCD05662353
[MOL File]

252049-10-8.mol
[Molecular Weight]

432.94
Chemical PropertiesBack Directory
[Melting point ]

>107°C (dec.)
[storage temp. ]

Store at +2°C to +8°C.
[solubility ]

DMSO (Slightly), Methanol (Slightly)
[form ]

Solid
[color ]

White to Pale Yellow
[Major Application]

peptide synthesis
[InChIKey]

SJFAFKDBWNFBCC-GKNLIIIVNA-N
[SMILES]

C(C1C2=CC=CC=C2C2C=CC=CC1=2)OC(=O)N[C@H](C(=O)O)CCCCN(C)C.Cl |&1:18,r|
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P280-P301+P312-P302+P352-P305+P351+P338
[WGK Germany ]

WGK 2
[HazardClass ]

IRRITANT
[HS Code ]

29225090
[Storage Class]

11 - Combustible Solids
Hazard InformationBack Directory
[Chemical Properties]

White to off white crystalline powder
[Uses]

Di-Me L-lysine derivative. The methylation of lysine in histone tails is a common posttranslational modification that functions in histone-regulated chromatin condensation, with binding of methylated lysine occurring in aromatic pockets on chromodomain proteins.
[Definition]

ChEBI: Fmoc-lys(ME)2-OH hcl is a member of fluorenes.
[General Description]

A novel derivative for the introduction of dimethyl-lysine during Fmoc SPPS. Ref [1] contains methods and protocols for the synthesis of arrays of histone-related peptides containing methylated arginine and lysine-residues.

The product number for this product was previously 04-12-1269.

To obtain a certificate of analysis (CoA) of a lot that begins with the letter “A”, please select the option in the right hand menu “Request a COA for Lot#s starting with A”.
[reaction suitability]

reaction type: Fmoc solid-phase peptide synthesis
Spectrum DetailBack Directory
[Spectrum Detail]

FMOC-LYS(ME)2-OH HCL(252049-10-8)1HNMR
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