04936

O-(6-Chlorbenzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium-hexafluorphosphat

≥98.0% (HPLC)

• Synonym(e): 1-[Bis-(dimethylamino)-methylen]-5-chlor-benzotriazolium-3-oxid-hexafluorophosphat, N,N,N′,N′-Tetramethyl-O-(6-chlor-1H-benzotriazol-1-yl)-uronium-hexafluorphosphat, HCTU
• Empirische Formel (Hill-System): C₁₁H₁₅ClF₆N₅OP
• CAS-Nummer: 330645-87-9
• Molekulargewicht: 413.69
• MDL-Nummer: MFCD04973268
• UNSPSC-Code: 12352101
• PubChem Substanz-ID: 329747994
• NACRES: NA.22

Eigenschaften

• Qualitätsniveau: 200
• Assay: ≥98.0% (HPLC)
• Form: powder
• Eignung der Reaktion: reaction type: Coupling Reactions
• Verunreinigungen: ≤0.5% water
• mp (Schmelzpunkt): 185-190 °C
• Anwendung(en): peptide synthesis
• Funktionelle Gruppe: amine; chloro
• SMILES String: ClC1=CC=C(N([C+](N(C)C)N(C)C)N=[N+]2[O-])C2=C1.F[P-](F)(F)(F)(F)F
• InChI: 1S/C11H15ClN5O.F6P/c1-15(2)11(16(3)4)18-17-10-7-8(12)5-6-9(10)13-14-17;1-7(2,3,4,5)6/h5-7H,1-4H3;/q+1;-1
• InChIKey: ZHHGTMQHUWDEJF-UHFFFAOYSA-N

Beschreibung

Anwendung

Reagent for:
Synthesis of near-infrared pH activatable fluorescent probes[1]
Synthesis of human β-amyloid by Fmoc chemistry[2]
Stereoselective Horner-Wadsworth-Emmons olefination[3]
Covalent ligation of fluorescent peptides to quantum dots[4]
Alkylation of human telomere sequence[5]

Sonstige Hinweise

Tandem Oligonucleotide Synthesis on Solid-Phase Supports for the Production of Multiple Oligonucleotides[6]

Sicherheitshinweise

• Piktogramme: GHS07
• Signalwort: Warning
• H-Sätze: H317
• P-Sätze: P261 - P272 - P280 - P302 + P352 - P333 + P313 - P362 + P364
• Gefahreneinstufungen: Skin Sens. 1A
• Lagerklassenschlüssel: 11 - Combustible Solids
• WGK: WGK 3
• Flammpunkt (°F): Not applicable
• Flammpunkt (°C): Not applicable