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About This Item
Empirical Formula (Hill Notation):
C11H15BClF4N5O
CAS Number:
Molecular Weight:
355.53
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352005
MDL number:
InChI
1S/C11H15ClN5O.BF4/c1-15(2)11(16(3)4)18-17-10-7-8(12)5-6-9(10)13-14-17;2-1(3,4)5/h5-7H,1-4H3;/q+1;-1
SMILES string
F[B-](F)(F)F.CN(C)C(\On1nnc2ccc(Cl)cc12)=[N+](/C)C
InChI key
GBGVQFJZGHBZMC-UHFFFAOYSA-N
assay
≥97.5% (HPLC), 98%
form
powder
reaction suitability
reaction type: Coupling Reactions
impurities
≤0.5% water
application(s)
peptide synthesis
functional group
amine, chloro
Application
Coupling reagent for:
- Synthesis via plate-based multiple parallel centrifugation synthesizer
- Solid-phase synthesis of cyclic gramicidin analogs
- Comparison of automatic multiple peptide synthesizers
- Solid-phase peptide coupling with lack of racemization
signalword
Danger
hcodes
Hazard Classifications
Flam. Sol. 1 - Skin Sens. 1A
supp_hazards
Storage Class
4.1B - Flammable solid hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Regulatory Information
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P Carvajal-Rondanelli et al.
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Previous work demonstrated that lysine homopeptides adopt a polyproline II (PPII) structure. Lysine homopeptides with odd number of residues, especially with 11 residues (K11), were capable of inhibiting the growth of a broader spectrum of bacteria than those with an
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Analytical and bioanalytical chemistry, 407(9), 2557-2567 (2015-02-01)
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