Search Thermo Fisher Scientific
Element Search
Structure Search
Thermo Scientific Chemicals
tert-Butylmagnesium chloride, 1M in MeTHF, Thermo Scientific Chemicals
Have Questions?
Change view
Catalog number H51164.AP
also known as H51164-AP
Price (USD)/ Each
760.65
Online exclusive
845.00 Save 84.35 (10%)
-
Quantity:
500 mL
Price (USD)/ Each
760.65
Online exclusive
845.00 Save 84.35 (10%)
tert-Butylmagnesium chloride, 1M in MeTHF, Thermo Scientific Chemicals
Catalog numberH51164.AP
Price (USD)/ Each
760.65
Online exclusive
845.00 Save 84.35 (10%)
-
Chemical Identifiers
CAS677-22-5
IUPAC Nametert-butyl(chloro)magnesium
Molecular FormulaC4H9ClMg
InChI KeyZDRJSYVHDMFHSC-UHFFFAOYSA-M
SMILESCC(C)(C)[Mg]Cl
View more
Specification Sheettert-Butylmagnesium chloride is a Grignard reagent used in organic synthesis. It is also involved in copper-catalyzed cross-coupling reaction with primary-alkyl halides.
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
tert-Butylmagnesium chloride is a Grignard reagent used in organic synthesis. It is also involved in copper-catalyzed cross-coupling reaction with primary-alkyl halides.
Solubility
Miscible with alcohol and water.
Notes
Air and moisture sensitive. Incompatible with oxidizing agents and bases.
tert-Butylmagnesium chloride is a Grignard reagent used in organic synthesis. It is also involved in copper-catalyzed cross-coupling reaction with primary-alkyl halides.
Solubility
Miscible with alcohol and water.
Notes
Air and moisture sensitive. Incompatible with oxidizing agents and bases.
RUO – Research Use Only
General References:
- Kerr, W. J.; Lindsay, D. M.; Patel, V. K.; Rajamanickam, M. Efficient methods for enol phosphate synthesis using carbon-centred magnesium bases. Org. Biomol. Chem. 2015, 13 (40), 10131-10135.
- Kamo, S.; Maruo, S.; Kuramochi, K.; Tsubaki, K. Synthesis of enantiomerically pure juglomycin C and NHAB. Tetrahedron 2015, 71 (21), 3478-3484.