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1,6-Dibromohexane, 97+%, Thermo Scientific Chemicals
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Catalog number A13417.36
also known as A13417-36
Price (USD)/ Each
91.65
Online exclusive
102.00 Save 10.35 (10%)
-
Quantity:
500 g
Price (USD)/ Each
91.65
Online exclusive
102.00 Save 10.35 (10%)
1,6-Dibromohexane, 97+%, Thermo Scientific Chemicals
Catalog numberA13417.36
Price (USD)/ Each
91.65
Online exclusive
102.00 Save 10.35 (10%)
-
Chemical Identifiers
CAS629-03-8
IUPAC Name1,6-dibromohexane
Molecular FormulaC6H12Br2
InChI KeySGRHVVLXEBNBDV-UHFFFAOYSA-N
SMILESBrCCCCCCBr
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Specifications
Specification Sheet
Specification SheetAppearance (Color)Clear colorless to pale yellow
FormLiquid
Identification (FTIR)Conforms
Assay (GC)≥97.0%
Refractive Index1.5050-1.5100 @ 20?C
1,6-Dibromohexane is used as a reagent in the synthesis of novel benzo[b]xanthone derivatives which have a potential antitumor activity. It is also used as a cross-linker for the cross-linking of glycuronans.
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
1,6-Dibromohexane is used as a reagent in the synthesis of novel benzo[b]xanthone derivatives which have a potential antitumor activity. It is also used as a cross-linker for the cross-linking of glycuronans.
Solubility
Miscible with ethanol, ether, benzene and chloroform. Immiscible with water.
Notes
Incompatible with strong oxidizing agents and strong bases.
1,6-Dibromohexane is used as a reagent in the synthesis of novel benzo[b]xanthone derivatives which have a potential antitumor activity. It is also used as a cross-linker for the cross-linking of glycuronans.
Solubility
Miscible with ethanol, ether, benzene and chloroform. Immiscible with water.
Notes
Incompatible with strong oxidizing agents and strong bases.
RUO – Research Use Only
General References:
- Gadgil, B.; Dmitrieva, E.; Damlin, P.; Aaritalo, T.; Kvamstrom, C. Redox reactions in a linear polyviologen derivative studied by in situ ESR/UV-vis-NIR spectroelectrochemistry. J. Solid State Electrochem. 2015, 19 (1), 77-83.
- Maeda, C.; Taniguchi, T.; Ogawa, K.; Ema, T. Bifunctional Catalysts Based on m-Phenylene-Bridged Porphyrin Dimer and Trimer Platforms: Synthesis of Cyclic Carbonates from Carbon Dioxide and Epoxides. Angew. Chem. 2015, 127 (1), 136-140.