Fmoc-D-lys-oh hcl

C21H25ClN2O4CAS 201002-47-3404.89 g/mol

Open in Covalent MOL file
OONHNH2OHOHCl
CarbamateCarboxylic acidPrimary amine

Properties

Molecular formula
C21H25ClN2O4
Molar mass
404.89 g/mol
Exact mass
404.1503 Da
logP
3.53Crippen estimate
Polar surface area
101.6 Ų
H-bond donors / acceptors
3 / 4
Rotatable bonds
8
Stereocentres
Rin SMILES atom order

Hazards

No GHS classification is on file for this compound. That is not evidence that it is harmless.

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Identifiers

CAS number
201002-47-3
SMILES
C1=CC=C2C(=C1)C(C3=CC=CC=C32)COC(=O)N[C@H](CCCCN)C(=O)O.Cl
InChIKey
MVMZFAIUUXYFGY-FSRHSHDFSA-N
InChI
InChI=1S/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-;/m1./s1

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Names and synonyms

1 names
  • (R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-6-aminohexanoic acid hydrochloride

Work with Fmoc-D-lys-oh hcl

Predict the NMR spectrum1H and 13C shifts with multiplicities Make a solutionWhat to weigh for any molarity and volume Check drug-likenessLipinski, Veber and lead-likeness Isotope patternExact mass and the mass spectrum pattern

Stereoisomers, salts and isotopologues

The same compound in another form: other stereochemistry, a salt or hydrate, the free acid or base, or an isotope-labelled version.

Fmoc-lys-oh105047-45-8Free base, enantiomer Nalpha-fmoc-L-lysine hydrochloride139262-23-0Enantiomer

Similar compounds

Fmoc-lys(me)2-oh hcl252049-10-874 % similar Fmoc-lys(fmoc)-oh78081-87-573 % similar Fmoc-D-nle-oh112883-41-772 % similar (2S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)hexanoic acid77284-32-372 % similar Fmoc-homoarg-oh776277-76-069 % similar (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-cyclopentylpropanoic acid371770-32-069 % similar Fmoc-L-norvaline135112-28-669 % similar (2R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)pentanoic acid144701-24-669 % similar

Tanimoto similarity of circular fingerprints over the whole catalogue.

All similar compounds

Elsewhere

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