Substance
ID:360772
O-(6-Chlorobenzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate
Names and Identifiers
Synonyms
HCTU1-[Bis(dimethylamino)methylen]-5-chlorobenzotriazolium 3-oxide hexafluorophosphateO-(6-氯-1-苯并三氮唑-1-基)-N,N,N′,N′-四甲基脲六氟磷酸酯O-(6-Chlorobenzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphateN,N,N′,N′-Tetramethyl-O-(6-chloro-1H-benzotriazol-1-yl)uronium hexafluorophosphate1-[双(二甲氨基)亚甲基]-5-氯苯并三唑鎓 3-氧化物六氟磷酸酯N,N,N′,N′-四甲基-O-(6-氯-1H-苯并三氮唑-1-基)脲六氟磷酸酯
IUPAC Traditional name
{[(6-chloro-1,2,3-benzotriazol-1-yl)oxy](dimethylamino)methylidene}dimethylazanium hexafluorophosphate
IUPAC name
hexafluoro-λ5-phosphanuide; {[(6-chloro-1H-1,2,3-benzotriazol-1-yl)oxy](dimethylamino)methylidene}dimethylazanium
Properties
Safety Information
German water hazard class
3
MSDS Link
Product Information
Impurities
≤0.5% water
Empirical Formula (Hill Notation)
C11H15ClF6N5OP
Purity
≥98.0% (HPLC)
Physical Property
Melting Point
185-190 °C
Molecule Details
Other Notes
Tandem Oligonucleotide Synthesis on Solid-Phase Supports for the Production of Multiple Oligonucleotides6
Application
Reagent for: Synthesis of near-infrared pH activatable fluorescent probes1 Synthesis of human β-amyloid by Fmoc chemistry2 Stereoselective Horner-Wadsworth-Emmons olefination3 Covalent ligation of fluorescent peptides to quantum dots4 Alkylation of human telomere sequence5
Tandem Oligonucleotide Synthesis on Solid-Phase Supports for the Production of Multiple Oligonucleotides6
Application
Reagent for: Synthesis of near-infrared pH activatable fluorescent probes1 Synthesis of human β-amyloid by Fmoc chemistry2 Stereoselective Horner-Wadsworth-Emmons olefination3 Covalent ligation of fluorescent peptides to quantum dots4 Alkylation of human telomere sequence5
Molecular Spectra
No Data Available
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References
No Data Available
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