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About This Item
Empirical Formula (Hill Notation):
C10H16BF4N3OS
CAS Number:
Molecular Weight:
313.12
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352005
MDL number:
InChI
1S/C10H16N3OS.BF4/c1-11(2)10(12(3)4)15-9-7-5-6-8-13(9)14;2-1(3,4)5/h5-8H,1-4H3;/q+1;-1
SMILES string
F[B-](F)(F)F.CN(C)C(\Sc1cccc[n+]1[O-])=[N+](/C)C
InChI key
LHLFXDQURZVFLK-UHFFFAOYSA-N
assay
≥95.0% (NMR)
reaction suitability
reaction type: Coupling Reactions
mp
109-114 °C
application(s)
peptide synthesis
storage temp.
−20°C
Application
Reagent for:
Synthesis of anticonvulsants
Solution and solid-phase peptide coupling
Conversion of carboxylic acids to Weinreb amides and N-methoxy or N-benzoxy amides
Rapid and high-yielding preparation of primary amides
Synthesis of anticonvulsants
Solution and solid-phase peptide coupling
Conversion of carboxylic acids to Weinreb amides and N-methoxy or N-benzoxy amides
Rapid and high-yielding preparation of primary amides
Other Notes
Very reactive peptide coupling reagent
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Find documentation for the products that you have recently purchased in the Document Library.
2-Mercaptopyridone 1-Oxide-Based Uronium Salts: New Peptide Coupling Reagents(1)(,)(2).
Miguel A. Bailén et al.
The Journal of organic chemistry, 64(24), 8936-8939 (2001-10-25)
F. Albericio et al.
Tetrahedron, 57, 9607-9607 (2001)
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