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Thermo Scientific Chemicals
Azidotri-n-butyltin(IV), 95%
CAS: 17846-68-3 | C12H27N3Sn | 332.079 g/mol
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Chemical Identifiers
CAS17846-68-3
IUPAC Nameazidotributylstannane
Molecular FormulaC12H29N3Sn
InChI KeyVJJINBNRYCPOOA-UHFFFAOYSA-N
SMILESN=[N+]=[N-].CCCC[SnH](CCCC)CCCC
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Specifications
Specification Sheet
Specification SheetInfrared spectrumConforms
Appearance (Color)Colorless to pale yellow
FormLiquid
Assay by NMR≥94.0%
Azidotri-n-butyltin(IV) is widely utilized as a reagent in the synthesis of tetrazolylbenzene compounds. It is employed in pharmaceutical research and involves synthesis of tetrazole derivatives, which is used to create angiotensin II receptor antagonists.
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
Azidotri-n-butyltin(IV) is widely utilized as a reagent in the synthesis of tetrazolylbenzene compounds. It is employed in pharmaceutical research and involves synthesis of tetrazole derivatives, which is used to create angiotensin II receptor antagonists.
Solubility
Miscible with toluene, hexane, acetonitrile and tetrahydrofuran.
Notes
Use in a fume hood. Keep container tightly closed in a dry and well-ventilated place. Incompatible with strong oxidizing agents.
Azidotri-n-butyltin(IV) is widely utilized as a reagent in the synthesis of tetrazolylbenzene compounds. It is employed in pharmaceutical research and involves synthesis of tetrazole derivatives, which is used to create angiotensin II receptor antagonists.
Solubility
Miscible with toluene, hexane, acetonitrile and tetrahydrofuran.
Notes
Use in a fume hood. Keep container tightly closed in a dry and well-ventilated place. Incompatible with strong oxidizing agents.
RUO – Research Use Only
General References:
- Jennepalli, S.; Pyne, S. G.; Keller, P. A. [60]Fullerenyl amino acids and peptides: a review of their synthesis and applications. RSC Adv. 2014, 4 (86), 46383-46398.
- Akhmetov, A. R.; Yarullin, I. R.; Tuktarov, A. R.; Dzhemilev, U. M. Reactions of fullerene C60 with organometallic azides. Tetrahedron Lett. 2014, 55 (28), 3747-3749.