Products for Research Use Only

N3-L-Dap (Boc) -OH

CAT: 0013-GTR19237553-01Size: 10 mgDry Ice: NoHazardous: No
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CAT#:0013-GTR19237553-01Size:10 mg
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Description
N3-L-Dap (Boc) -OH is an azide-functionalized click chemistry reagent suitable for CuAAC and SPAAC reactions. It enables efficient bioconjugation for applications in chemical biology, such as labeling biomolecules in vitro and developing probes for in vivo imaging studies.
CAS Number
1932432-15-9
Field of Research
Cell Biology
Smiles
[C@@H] (CNC (OC (C) (C) C) =O) (N=[N+]=[N-]) C (O) =O
Molecular Formula
C8H14N4O4
Molecular Weight
230.22
Storage Conditions
-20°C
Notes
For research use only.

Chemical Information

N3-L-Dap(Boc)-OH
CAS Number1932432-15-9
PubChem CID75409964
IUPAC Name(2S)-2-azido-3-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid
Molecular FormulaC8H14N4O4
Molecular Weight230.22
XLogP1.6
Topological Polar Surface Area90
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count6
Rotatable Bond Count6
Heavy Atom Count16
Formal Charge0
Complexity316
SMILES
CC(C)(C)OC(=O)NC[C@@H](C(=O)O)N=[N+]=[N-]
InChI
InChI=1S/C8H14N4O4/c1-8(2,3)16-7(15)10-4-5(6(13)14)11-12-9/h5H,4H2,1-3H3,(H,10,15)(H,13,14)/t5-/m0/s1
InChIKey
IVADUQQDYTXXQS-YFKPBYRVSA-N
Chemical Structure
2D Structure
2D structure of N3-L-Dap(Boc)-OH
CAS: 1932432-15-9
CID: 75409964
Formula: C8H14N4O4
MW: 230.22
Interactive 3D Structure
Loading 3D structure...
Computed Properties
PropertyValue
Molecular Weight230.22
XLogP31.6
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count6
Rotatable Bond Count6
Exact Mass230.10150494
Monoisotopic Mass230.10150494
Topological Polar Surface Area90 Ų
Heavy Atom Count16
Formal Charge0
Complexity316
Isotope Atom Count0
Defined Atom Stereocenter Count1
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Covalently-Bonded Unit Count1
Compound Is CanonicalizedYes