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H-Lys(Boc)-OH

CAS No.:
2418-95-3
Catalog Number:
AG0035DK
Molecular Formula:
C11H22N2O4
Molecular Weight:
246.3034
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1g
98%
In Stock USA
United States
$13
- +
5g
98%
In Stock USA
United States
$17
- +
25g
≥97%
In Stock USA
United States
$60
- +
100g
98%
In Stock USA
United States
$169
- +
500g
98%
In Stock USA
United States
$525
- +
Product Description
Catalog Number:
AG0035DK
Chemical Name:
H-Lys(Boc)-OH
CAS Number:
2418-95-3
Molecular Formula:
C11H22N2O4
Molecular Weight:
246.3034
MDL Number:
MFCD00037221
IUPAC Name:
(2S)-2-amino-6-[(2-methylpropan-2-yl)oxycarbonylamino]hexanoic acid
InChI:
InChI=1S/C11H22N2O4/c1-11(2,3)17-10(16)13-7-5-4-6-8(12)9(14)15/h8H,4-7,12H2,1-3H3,(H,13,16)(H,14,15)/t8-/m0/s1
InChI Key:
VVQIIIAZJXTLRE-QMMMGPOBSA-N
SMILES:
O=C(OC(C)(C)C)NCCCC[C@@H](C(=O)O)N
Properties
Complexity:
261  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
1  
Defined Bond Stereocenter Count:
0
Exact Mass:
246.158g/mol
Formal Charge:
0
Heavy Atom Count:
17  
Hydrogen Bond Acceptor Count:
5  
Hydrogen Bond Donor Count:
3  
Isotope Atom Count:
0
Molecular Weight:
246.307g/mol
Monoisotopic Mass:
246.158g/mol
Rotatable Bond Count:
8  
Topological Polar Surface Area:
102A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
-1.6  
Literature
Title Journal
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Genetically encoded norbornene directs site-specific cellular protein labelling via a rapid bioorthogonal reaction. Nature chemistry 20120205
Well-defined homopolypeptides, copolypeptides, and hybrids of poly(l-proline). Biomacromolecules 20110613
Engineered diubiquitin synthesis reveals Lys29-isopeptide specificity of an OTU deubiquitinase. Nature chemical biology 20101001
Synthesis of a l-lysine-based alternate alpha,epsilon-peptide: a novel linear polycation with nucleic acids-binding ability. International journal of pharmaceutics 20100915
Synthesis and evaluation of a library of 2,5-bisdiamino-benzoquinone derivatives as probes to modulate protein-protein interactions in prions. Bioorganic & medicinal chemistry letters 20100315
Recognition of non-alpha-amino substrates by pyrrolysyl-tRNA synthetase. Journal of molecular biology 20090206
Multistep engineering of pyrrolysyl-tRNA synthetase to genetically encode N(epsilon)-(o-azidobenzyloxycarbonyl) lysine for site-specific protein modification. Chemistry & biology 20081124
Adding l-lysine derivatives to the genetic code of mammalian cells with engineered pyrrolysyl-tRNA synthetases. Biochemical and biophysical research communications 20080711
Biochemical characterisation of recombinant Streptomyces pristinaespiralis L-lysine cyclodeaminase. Biochimie 20070501
Development of a mechanism-based assay for tissue transglutaminase--results of a high-throughput screen and discovery of inhibitors. Analytical biochemistry 20050315
Isolation and characterization of a new advanced glycation endproduct of dehydroascorbic acid and lysine. Biochimica et biophysica acta 20030317
Evidence that malondialdehyde-derived aminoenimine is not a fluorescent age pigment. Chemical research in toxicology 20010501
Properties