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Benzylmagnesium chloride(1M THF)

$ 57.00 /1KG

Min. Order1KG
Purity99%
Cas No6921-34-2
Supply Ability5000 tons
Update time2023-01-30

Hebei Duling International Trade Co. LTD

Hebei Duling International Trade Co. LTD

2YR

China

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Chemical Properties

Product Name	Benzylmagnesium chloride(1M THF)
CAS No	6921-34-2
EC-No	230-039-0
Min. Order	1KG
Purity	99%
Supply Ability	5000 tons
Release date	2023/01/30

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Email: sales02@hbduling.cn

Product Name:	Benzylmagnesium chloride
Synonyms:	chloro(phenylmethyl)-magnesiu;BENZYLMAGNESIUM CHLORIDE, 1.0M SOLUTION IN DIETHYL ETHER;BENZYLMAGNESIUM CHLORIDE, 2.0M SOLUTION IN TETRAHYDROFURAN;BENZYLMAGNESIUM CHLORIDE SOLUTION, ~1.3 M IN THF;BENZYLMAGNESIUM CHLORIDE SOL., ~1 M IN D IETHYL ETHER;Benzylmagnesium Chloride 0.9 M In Dibutyl Ether;Benzylmagnesium Chloride 1.0 M In Tetrahydrofuran;Benzylmagnesium Chloride 1.5 M In Tetrahydrofuran
CAS:	6921-34-2
MF:	C7H7ClMg
MW:	150.89
EINECS:	230-039-0
Product Categories:	grignard reagent;Alkyl;Classes of Metal Compounds;Grignard Reagents;Grignard Reagents;Organometallic Reagents;Grignard Reagents & Alkyl Metals;Mg (Magnesium) Compounds;Synthetic Organic Chemistry;Typical Metal Compounds
Mol File:	6921-34-2.mol

Chemical Properties	Light gray to dark amber-grey slurry or solution
Uses	Benzyl magnesium chloride is used as a Grignard reagent in greener solvent, 2-methyltetrahydrofuran (2-MeTHF). It is also used as organic chemical synthesis intermediate.
Uses	Benzylmagnesium chloride (Grignard reagent) can be used as an alkylating reagent: For alkylating quinolyl-functionalized Cp?chromium(III) complexes which are used as precursors for the preparation of active olefin polymerization catalysts. In the synthesis of 2,3-disubstituted benzopyran-4-ones, 6-chloro-8-methylpurine derivative, and phenylalanine derivatives.
Application	Benzylmagnesium chloride (Grignard reagent) can be used as an alkylating reagent: For alkylating quinolyl-functionalized Cp?chromium(III) complexes which are used as precursors for the preparation of active olefin polymerization catalysts. In the synthesis of 2,3-disubstituted benzopyran-4-ones, 6-chloro-8-methylpurine derivative, and phenylalanine derivatives.
General Description	This product has been enhanced for energy efficiency.
Research	Grignard reagents are organometallic compounds discovered by a French chemist, Victor Grignard in 1900. These compounds can be obtained as a formula “RMgX” by the reaction of halogenated hydrocarbons with magnesium metal in anhydrous solvents such as diethyl ether,1) and have been widely used in organic synthesis. Grignard reagents are usually used as solutions, and they are typically grayish white ~ light brown clear solutions. They generally exist in an equilibrium between alkyl magnesium halides (RMgX) and dialkyl magnesium (R2Mg), which form equilibrium mixtures with complicated compositions (called “Schlenk equilibrium”).2) Furthermore, some of these species may cause precipitation due to their lower solubility. However, there is no problem in actual use. In the case of precipitation being formed: Please use it after gently shaking the bottle to fully disperse the suspension (If the amount of precipitation is very small, you can use the top clear layer of the suspension). Especially in cold conditions such as in winter, a large amount of precipitate may frequently form. In this case, please use it after crushing the solid with a dried glass stick. Alternatively, you can also use it the following. The bottle is put into a plastic bag and soaking in a water bath with warming at 40 degree C to dissolve the solid. Please be careful of volatilization of the organic solvent when the bottle is unsealing.

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