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5674-02-2

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5674-02-2 Usage

Chemical Properties

Dark brown liquid

Check Digit Verification of cas no

The CAS Registry Mumber 5674-02-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,7 and 4 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5674-02:
(6*5)+(5*6)+(4*7)+(3*4)+(2*0)+(1*2)=102
102 % 10 = 2
So 5674-02-2 is a valid CAS Registry Number.
InChI:InChI=1/C4H9.ClH.Mg/c1-4(2)3;;/h4H,1H2,2-3H3;1H;/q;;+1/p-1/rC4H9Mg.ClH/c1-4(2)3-5;/h4H,3H2,1-2H3;1H/q+1;/p-1

5674-02-2 Well-known Company Product Price

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  • Aldrich

  • (479683)  Isobutylmagnesiumchloridesolution  2.0 M in THF

  • 5674-02-2

  • 479683-100ML

  • 568.62CNY

  • Detail
  • Aldrich

  • (479683)  Isobutylmagnesiumchloridesolution  2.0 M in THF

  • 5674-02-2

  • 479683-1L

  • 3,098.16CNY

  • Detail

5674-02-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name ISOBUTYLMAGNESIUM CHLORIDE

1.2 Other means of identification

Product number -
Other names magnesium,2-methanidylpropane,chloride

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:5674-02-2 SDS

5674-02-2Relevant articles and documents

Active Magnesium from Catalytically Prepared Magnesium Hydride or from Magnesium Anthracene and its Uses in the Synthesis

Bartmann, Ekkehard,Bogdanovic, Borislav,Janke, Nikolaus,Liao, Shijan,Schlichte, Klaus,et al.

, p. 1517 - 1528 (2007/10/02)

Highly reactive, pyrophoric forms of magnesium with specific surface areas of 20-109 m2/g (Mg*) can be generated by the dehydrogenation of catalytically prepared magnesium hydride (MgH2*) or by decomposition of magnesium anthracene * 3 THF (4).The decomposition of 4, with recovery of anthracene and THF, may be accomplished both thermally and by ultrasound in an organic solvent (toluene, n-heptane) or thermally in the solid state in vacuo.Mg* obtained by the latter method exhibits only weak reflections in the X-ray powder diagram and has, in comparison to other mentioned Mg* species, the highest reactivity toward hydrogen.Diverse Grignard compounds can be prepared under mild conditions (* from MgH2* or 4.The cleavage of THF with formation of 1-oxa-2-magnesiacyclohexane (2) is possible by employing Mg* from NgH2* or 4.

Process for using finely divided highly reactive magnesium

-

, (2008/06/13)

The present invention relates to a process for preparing a finely divided, highly reactive magnesium from magnesium hydride, magnesium anthracene and/or its derivatives or magnesium butadiene and/or its alkyl or phenyl derivatives, which process is characterized in that the respective magnesium-containing compound is thermally decomposed at a pressure from 10-6 to 1 bar, the decomposition being carried out in the presence of a co-reactant of a consecutive reaction, or such co-reactant being added only after completion of the precipitation of the magnesium, or in the absence of such co-reactant, the magnesium obtained by said decomposition being isolated as a powder, and to the use of the finely divided, highly reactive magnesium for inserting magnesium into poorly reactive C--X bonds, wherein X denotes heteroatoms such as halogen, oxygen, sulfur, nitrogen, phosphorus, and the resulting organomagnesium compound may be used in a consecutive reaction according to a per se known method, and for the reversible preparation of active magnesium hydride by reaction with molecular hydrogen at a pressure of from 1 to 2 bar and at a temperature of from 150° C. to 250° C.

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