O-(7-Aza-1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate, 99%, Thermo Scientific Chemicals
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O-(7-Aza-1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate, 99%, Thermo Scientific Chemicals
O-(7-Aza-1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate, 99%, Thermo Scientific Chemicals
O-(7-Aza-1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate, 99%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

O-(7-Aza-1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate, 99%, Thermo Scientific Chemicals

CAS: 148893-10-1 | C10H15F6N6OP | 380.24 g/mol
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Catalog NumberQuantity
ALFH26082.065 g
Catalog number ALFH26082.06
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Quantity:
5 g
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Chemical Identifiers
CAS886-38-4
IUPAC Namediphenylcycloprop-2-en-1-one
Molecular FormulaC15H10O
InChI KeyHCIBTBXNLVOFER-UHFFFAOYSA-N
SMILESO=C1C(=C1C1=CC=CC=C1)C1=CC=CC=C1
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SpecificationsSpecification SheetSpecification Sheet
Appearance (Form)Powder or crystalline powder
Appearance (Color)Almost white to light orange-pink to beige
Melting point117°C to 121°C
Infrared spectrumConforms
HPLC>=97.5 %
O-(7-Aza-1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate is a coupling reagent and used as an additive in peptide synthesis., It is also involved efficiently to speed up the coupling process and reduces the loss of chiral integrity.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
O-(7-Aza-1H-benzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate is a coupling reagent and used as an additive in peptide synthesis., It is also involved efficiently to speed up the coupling process and reduces the loss of chiral integrity.

Solubility
Soluble in acetonitrile. Insoluble in water.

Notes
Moisture sensitive. Incompatible with oxidizing agents and highly acidic or alkaline materials.
RUO – Research Use Only

General References:

  1. Yoshida, M.; Sasahara, K. I.; Doi, T. Total synthesis of cyclodepsipeptide spiruchostatin A on silyl-linked polymer-support. Tetrahedron 2015, 71 (40), 7647-7653.
  2. Xie, Y.; Yu, C.; Li, T.; Tu, S.; Yao, C. An NHC-Catalyzed In Situ Activation Strategy to β-Functionalize Saturated Carboxylic Acid: An Enantioselective Formal [3+ 2] Annulation for Spirocyclic Oxindolo-γ-butyrolactones. Chem. Eur. J. 2015, 21 (14), 5355-5359.