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线性分子式:
Mg(ClO4)2
化学文摘社编号:
分子量:
223.21
UNSPSC Code:
12352300
PubChem Substance ID:
EC Number:
233-108-3
MDL number:
Assay:
≥99.0% (calc. based on dry substance, KT)
Form:
free flowing powder
InChI key
MPCRDALPQLDDFX-UHFFFAOYSA-L
InChI
1S/2ClHO4.Mg/c2*2-1(3,4)5;/h2*(H,2,3,4,5);/q;;+2/p-2
SMILES string
[Mg++].[O-]Cl(=O)(=O)=O.[O-]Cl(=O)(=O)=O
grade
puriss.
assay
≥99.0% (calc. based on dry substance, KT)
form
free flowing powder
quality
free-flowing powder
impurities
≤8% water
storage temp.
room temp
Quality Level
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General description
Magnesium perchlorate (Mg(ClO4)2) is widely used as drying agent for gases. It can remove water from gases (with no organic contaminants) at the rate of 0.001mgwater/l.
Application
干燥管的填充剂(尤其是用于元素分析)
Magnesium perchlorate (Mg(ClO4)2) may be employed as a catalyst in the following studies:
- Preparation of a-aminophosphonates.
- Enantioselective Diels-Alder reaction between cyclopentadiene and 3-acryloyl-1,3-oxazolin-2-one.
- Preparation of imines and phenylhydrazones.
- Protection of alcohols in the form of t-butyl ethers.
signalword
Danger
hcodes
Hazard Classifications
Eye Irrit. 2 - Ox. Sol. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
5.1A - Strongly oxidizing hazardous materials
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
法规信息
危险化学品
此项目有
Eagleson M.
Concise Encyclopedia Chemistry, 343-343 (1994)
Magnesium perchlorate as an efficient catalyst for the synthesis of imines and phenylhydrazones.
Chakraborti AK, et al.
Tetrahedron Letters, 45(41), 7641-7644 (2004)
Giuseppe Bartoli et al.
Organic letters, 7(3), 427-430 (2005-01-28)
[reaction: see text] A new mild method for protecting alcohols as t-butyl ethers is reported. The reaction proceeds with Mg(ClO4)2 and Boc2O and shows general applicability. The deprotection of t-butyl ethers has also been revisited. Preliminary results indicate the CeCl3
The first enantioselective synthesis of both Diels-Alder enantiomers with the same bis (oxazoline)-magnesium perchlorate chiral catalyst.
Desimoni G, et al.
Tetrahedron Letters, 37(17), 3027-3030 (1996)
F Javier Céspedes-Guirao et al.
The Journal of organic chemistry, 74(16), 5871-5880 (2009-07-29)
Zinc phthalocyanine-perylenebisimide pentameric arrays, ZnPc(PDI)(4) 1 and 2, have been synthesized. ZnPc(PDI)(4) 1 has no substituents in the PDI bay positions, while ZnPc(PDI)(4) 2 presents four phenoxy groups in the bay positions of each perylene. In both cases, the PDI
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