InChI
1S/Mg
SMILES string
[Mg]
InChI key
FYYHWMGAXLPEAU-UHFFFAOYSA-N
vapor pressure
1 mmHg ( 621 °C)
form
turnings
autoignition temp.
950 °F
composition
anhydrous tetrahydrofuran, 37.5 mmol
reaction suitability
reagent type: reductant
resistivity
4.46 μΩ-cm, 20°C
bp
1090 °C (lit.)
mp
648 °C (lit.)
density
1.74 g/mL at 25 °C (lit.)
Quality Level
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Application
Magnesium turnings (Mg) can be used to prepare reactive organomagnesium compounds (Grignard reagents, GR) by reacting with alkyl, allyl, vinyl, or aryl halides. These GR reagents are widely used in organic synthesis to produce useful chemical intermediates. Mg can also be used to prepare tetraisopropyl- and tetrabutyl-distibane by dehalogenation of diisopropyl- and dibutyl-antinomy bromide, respectively.
Other Notes
产品为制备的有机镁试剂的 0.5M 溶液,40% 顶空。
Legal Information
Sure/Seal is a trademark of Sigma-Aldrich Co. LLC
signalword
Danger
Hazard Classifications
Acute Tox. 4 Oral - Carc. 2 - Eye Irrit. 2 - Flam. Liq. 2 - Self-heat. 1 - STOT SE 3
target_organs
Respiratory system
supp_hazards
存储类别
4.2 - Pyrophoric and self-heating hazardous materials
wgk
WGK 1
flash_point_f
1.4 °F - closed cup
flash_point_c
-17.0 °C - closed cup
法规信息
危险化学品
此项目有
Reduktion von isopropyl-und butylantimonbromiden mit magnesium
Breunig HJ and KW
Journal of Organometallic Chemistry, 186(1), C5-C8 (1980)
Mechanical activation of magnesium turnings for the preparation of reactive Grignard reagents
Baker KV, et al.
The Journal of Organic Chemistry, 56(2), 698-703 (1991)
Titanium-magnesium-assisted scission of 1, 4-bis (trimethylsilyl)-1, 3-butadiyne: synthesis and structure of a titanium (III) tweezer complex,[(. eta. 5-C5HMe4) 2Ti (. eta. 1-C. tplbond. CSiMe3) 2][Mg (THF) Cl]
Troyanov SI, et al.
Organometallics, 12(7), 2820-2824 (1993)
Jochen Halfar et al.
Proceedings of the National Academy of Sciences of the United States of America, 110(49), 19737-19741 (2013-11-20)
Northern Hemisphere sea ice has been declining sharply over the past decades and 2012 exhibited the lowest Arctic summer sea-ice cover in historic times. Whereas ongoing changes are closely monitored through satellite observations, we have only limited data of past
Shuvendu Biswas et al.
Nature chemistry, 5(7), 613-620 (2013-06-22)
The development of nanocarriers that selectively release guest molecules on sensing a particular biological signal is being actively pursued in nanomedicine for diagnostic and therapeutic purposes. Here we report a protein-based nanocarrier that opens in the presence of intracellular adenosine-5'-triphosphate
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