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Tris(3,6-dioxaheptyl)amine, 95%, Thermo Scientific Chemicals
Catalog number: L13544.22
100 g, Each
Thermo Scientific Chemicals
Tris(3,6-dioxaheptyl)amine, 95%, Thermo Scientific Chemicals
Catalog number: L13544.22
100 g, Each
Quantity
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Chemical Identifiers
CAS
70384-51-9
IUPAC Name
8-[2-(2-methoxyethoxy)ethyl]-2,5,11,14-tetraoxa-8-azapentadecane
Molecular Formula
C15H33NO6
InChI Key
XGLVDUUYFKXKPL-UHFFFAOYSA-N
SMILES
COCCOCCN(CCOCCOC)CCOCCOC
Specifications
Specification SheetForm
Liquid
Refractive Index
1.4465-1.4490 @ 20?C
Appearance (Color)
Clear pale yellow to yellow to orange to brown
Assay (GC)
≥94.0%
Description
Tris(3,6-dioxaheptyl)amine acts as a phase transfer catalyst used in the preparation of 1,3-dideaza-2'-deoxyadenosine and related benzimidazole 2'-deoxyribonucleosides. It is also used as an intermediate in the synthesis of telithromycin. Further, it is used in the oxidation of arylmethanols under phase-transfer conditions. In addition to this, it acts as a cryptand during phase-transfer glycosylation of 2-amino-4-methoxy-7H-pyrrolo[2,3-d]pyrimidine.
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
Tris(3,6-dioxaheptyl)amine acts as a phase transfer catalyst used in the preparation of 1,3-dideaza-2′-deoxyadenosine and related benzimidazole 2′-deoxyribonucleosides. It is also used as an intermediate in the synthesis of telithromycin. Further, it is used in the oxidation of arylmethanols under phase-transfer conditions. In addition to this, it acts as a cryptand during phase-transfer glycosylation of 2-amino-4-methoxy-7H-pyrrolo[2,3-d]pyrimidine.
Solubility
Miscible with water.
Notes
Air sensitive and hygroscopic. Incompatible strong oxidizing agents and strong acids.
Tris(3,6-dioxaheptyl)amine acts as a phase transfer catalyst used in the preparation of 1,3-dideaza-2′-deoxyadenosine and related benzimidazole 2′-deoxyribonucleosides. It is also used as an intermediate in the synthesis of telithromycin. Further, it is used in the oxidation of arylmethanols under phase-transfer conditions. In addition to this, it acts as a cryptand during phase-transfer glycosylation of 2-amino-4-methoxy-7H-pyrrolo[2,3-d]pyrimidine.
Solubility
Miscible with water.
Notes
Air sensitive and hygroscopic. Incompatible strong oxidizing agents and strong acids.
RUO – Research Use Only
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