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1-Bromoundecane, 98%
CAS: 693-67-4 | C11H23Br | 235.209 g/mol
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Catalog number ALFA14333.22
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Quantity:
100 g
Specifications
Chemical Name or Material1-Bromoundecane
CAS693-67-4
Health Hazard 1H315-H319-H332-H335
Health Hazard 2GHS H Statement
H315-H319-H335
Causes skin irritation.
Causes serious eye irritation.
May cause respiratory irritation.
H315-H319-H335
Causes skin irritation.
Causes serious eye irritation.
May cause respiratory irritation.
Health Hazard 3P261-P264b-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313-P362-P501c
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1-Bromoundecane is used in the preparation of Grignard reagent by reacting with Mg in THF (tetrahydrofuran). It is an important raw material and intermediate used in organic synthesis, pharmaceuticals, dyes and agrochemicals.
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-Bromoundecane is used in the preparation of Grignard reagent by reacting with Mg in THF (tetrahydrofuran). It is an important raw material and intermediate used in organic synthesis, pharmaceuticals, dyes and agrochemicals.
Solubility
Insoluble in water.
Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Incompatible with strong oxidizing agents and strong bases.
1-Bromoundecane is used in the preparation of Grignard reagent by reacting with Mg in THF (tetrahydrofuran). It is an important raw material and intermediate used in organic synthesis, pharmaceuticals, dyes and agrochemicals.
Solubility
Insoluble in water.
Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Incompatible with strong oxidizing agents and strong bases.
RUO – Research Use Only
General References:
- Kumaraswamy G.; Markondaiah B. Enantioselective total synthesis of (-)-tetrahydrolipstatin using Oppolzer’s sultam directed aldol reaction. Tetrahedron Lett. 2008, 49 (2), 327-330.
- Jean-François Peyrata.; Bruno Figadèrea.; André Cavé. Halide Exchange: Preparation of Alkyl Chlorides. Synthetic Communications: An International Journal for Rapid Communication of Synthetic Organic Chemistry. 1996, 26 (24), 4563-4567.