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1-Iododecane, 98%, stab. with copper
CAS: 2050-77-3 | C10H21I | 268.18 g/mol
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Catalog number A16173.30
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277.65
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Quantity:
250 g
Price (USD)
277.65
Online Exclusive
308.00Save 30.35 (10%)
Each
Chemical Identifiers
CAS2050-77-3
IUPAC Name1-iododecane
Molecular FormulaC10H21I
InChI KeySKIDNYUZJPMKFC-UHFFFAOYSA-N
SMILESCCCCCCCCCCI
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Specifications
Specification Sheet
Specification SheetAppearance (Color)Clear colorless to yellow
Assay (GC)≥97.5%
Refractive Index1.4830-1.4870 @ 20?C
Identification (FTIR)Conforms
StabilizerCopper Wire
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1-Iododecane is used as a precursor to prepare 9-nonadecanone through palladium-catalyzed carbonylative cross-coupling reaction with 9-octyl-9-borabicyclo[3.3.l]nonane. It is also used as an intermediate in organic synthesis.
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
1-Iododecane is used as a precursor to prepare 9-nonadecanone through palladium-catalyzed carbonylative cross-coupling reaction with 9-octyl-9-borabicyclo[3.3.l]nonane. It is also used as an intermediate in organic synthesis.
Solubility
Immiscible with water.
Notes
Light sensitive. Incompatible with strong oxidizing agents and strong bases. Keep the container tightly closed.
1-Iododecane is used as a precursor to prepare 9-nonadecanone through palladium-catalyzed carbonylative cross-coupling reaction with 9-octyl-9-borabicyclo[3.3.l]nonane. It is also used as an intermediate in organic synthesis.
Solubility
Immiscible with water.
Notes
Light sensitive. Incompatible with strong oxidizing agents and strong bases. Keep the container tightly closed.
RUO – Research Use Only
General References:
- Strawsine, L. M.; Sengupta, A.; Raghavachari, K.; Peters, D. G. Direct Reduction of Alkyl Monohalides at Silver in Dimethylformamide: Effects of Position and Identity of the Halogen. ChemElectroChem 2015, 2 (5), 726-736.
- Bilbao, N.; Vázquez-González, V.; Aranda, M. T.; González-Rodríguez, D. Synthesis of 5-/8-Halogenated or Ethynylated Lipophilic Nucleobases as Potential Synthetic Intermediates for Supramolecular Chemistry. Eur. J. Org. Chem. 2015, 2015 (32), 7160-7175.