ChemicalBook--->CAS DataBase List--->139262-23-0

139262-23-0

139262-23-0 Structure

139262-23-0 Structure
IdentificationMore
[Name]

Nalpha-Fmoc-L-lysine hydrochloride
[CAS]

139262-23-0
[Synonyms]

FMOC-L-LYSINE HYDROCHLORIDE
FMOC-LYSINE HCL
FMOC-LYS-OH HCL
Fmoc-Lys-OH hydrochloride
N-ALPHA-(9-FLUORENYLMETHOXYCARBONYL)-L-LYSINE HYDROCHLORIDE
N-ALPHA-FMOC-L-LYSINE, HCL
N(ALPHA)-FMOC-L-LYSINE HYDROCHLORIDE
Nα-Fmoc-L-lysine hydrochloride
nα-fmoc-l-lysine hydrochloride
Fmoc-L-Lys-OH·HCl
Nalpha-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-lysine Hydrochloride
[Molecular Formula]

C21H25ClN2O4
[MDL Number]

MFCD00190889
[Molecular Weight]

404.89
[MOL File]

139262-23-0.mol
Questions And AnswerBack Directory
[Synthesis]

The protected amino acid derivative (2 mg) was placed in a 1.5 mL glass vial with a screw cap. The appropriate acid solution (1 mL) and 0.1 M HCl were added to the HFIP. The reaction mixture was incubated at room temperature for 240 min, and the product Fmoc-Lys-OH hydrochloride was obtained by RT-HPLC and MALDI-TOF or ESI HR mass spectrometry.

Chemical PropertiesBack Directory
[refractive index ]

-11.0 ° (C=1, DMF)
[storage temp. ]

2-8°C
[solubility ]

Soluble in dimethyl formamide (0.3g in 2ml).
[form ]

powder to crystal
[color ]

White to Almost white
[BRN ]

8663370
[Major Application]

peptide synthesis
[InChIKey]

MVMZFAIUUXYFGY-FYZYNONXSA-N
[SMILES]

C(C1C2=CC=CC=C2C2C=CC=CC1=2)OC(=O)N[C@H](C(=O)O)CCCCN.Cl |&1:18,r|
[CAS DataBase Reference]

139262-23-0(CAS DataBase Reference)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[Safety Statements ]

24/25
[WGK Germany ]

3
[REACH Registrations]

Active
[HS Code ]

29242990
[Storage Class]

11 - Combustible Solids
Hazard InformationBack Directory
[Description]

Fmoc-Lys-OH hydrochloride is a cleavable ADC linker used to synthesize antibody-drug conjugates (ADCs). Fmoc-Lys-OH hydrochloride is also an alkyl chain-based PROTAC linker that can be used to synthesize PROTACs.
[Chemical Properties]

White solid
[Uses]

It is used as an active pharmaceutical intermediate and in the synthesis of nε-(7-diethylaminocoumarin-3-carboxyl)- and nε-(7-methoxycoumarin-3-carboxyl)-l-fmoc lysine as tools for protease cleavage detection by fluorescence.
[reaction suitability]

reaction type: Fmoc solid-phase peptide synthesis
[IC 50]

Non-cleavable Linker
Spectrum DetailBack Directory
[Spectrum Detail]

Fmoc-Lys-OH hydrochloride(139262-23-0)1HNMR
Well-known Reagent Company Product InformationBack Directory
[Sigma Aldrich]

139262-23-0(sigmaaldrich)
[TCI AMERICA]

Nalpha-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-lysine Hydrochloride,>94.0%(T)(139262-23-0)
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