13132-23-5 Usage
Uses
Used in Organic Synthesis:
NEOPENTYLMAGNESIUM CHLORIDE is used as a reagent for the formation of carbon-carbon and carbon-heteroatom bonds in organic synthesis. Its application is crucial in the preparation of various organic compounds due to its efficiency and versatility.
Used in Grignard Reactions:
In the field of organic chemistry, NEOPENTYLMAGNESIUM CHLORIDE is used as a key reagent in Grignard reactions. It facilitates the addition of a magnesium halide to a carbonyl compound, leading to the formation of new carbon-carbon bonds, which is essential for the synthesis of complex organic molecules.
Used in Laboratory and Industrial Settings:
NEOPENTYLMAGNESIUM CHLORIDE is utilized in both laboratory and industrial settings for the preparation of a wide range of organic compounds. Its broad application in these settings underscores its importance in the field of organic synthesis and chemical manufacturing.
Check Digit Verification of cas no
The CAS Registry Mumber 13132-23-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,1,3 and 2 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 13132-23:
(7*1)+(6*3)+(5*1)+(4*3)+(3*2)+(2*2)+(1*3)=55
55 % 10 = 5
So 13132-23-5 is a valid CAS Registry Number.
InChI:InChI=1/C5H11.ClH.Mg/c1-5(2,3)4;;/h1H2,2-4H3;1H;/q-1;;+2/p-1
13132-23-5Relevant academic research and scientific papers
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.
