2031-62-1 Usage
Description
Diethoxymethylsilane, a colorless clear liquid, is an organosilicon compound known for its versatile applications in various chemical reactions and industries.
Uses
Used in Chemical Synthesis:
Diethoxymethylsilane is used as a reagent for the preparation of N,N'-methylsilanediyl-bis-phthalimide by reacting with phthalimide. Diethoxymethylsilane finds applications in the synthesis of various organic compounds and materials.
Used in Carbonyl Compound Reduction:
Diethoxymethylsilane serves as a reagent in the selective reduction of carbonyl compounds, which is a crucial step in the synthesis of numerous organic molecules and pharmaceuticals.
Used in Hydrosilylation of Alkenes:
In the field of organic chemistry, Diethoxymethylsilane is utilized for the hydrosilylation of alkenes, a reaction that involves the addition of a silane across a carbon-carbon double bond, leading to the formation of new carbon-silicon bonds.
Used in Tandem Reductive Aldol Reaction:
Diethoxymethylsilane is employed in tandem reductive aldol reactions, which are multi-step processes that involve the formation of new carbon-carbon bonds and are essential for constructing complex molecular structures.
Used in Rhodium-Catalyzed Silylcarbocyclization:
This organosilicon compound is also used in the rhodium-catalyzed silylcarbocyclization, a reaction that leads to the formation of cyclic compounds with the assistance of a rhodium catalyst, which is vital for the synthesis of various pharmaceuticals and natural products.
Flammability and Explosibility
Flammable
Check Digit Verification of cas no
The CAS Registry Mumber 2031-62-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,3 and 1 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2031-62:
(6*2)+(5*0)+(4*3)+(3*1)+(2*6)+(1*2)=41
41 % 10 = 1
So 2031-62-1 is a valid CAS Registry Number.
InChI:InChI=1/C5H13O2Si/c1-4-6-8(3)7-5-2/h4-5H2,1-3H3
2031-62-1Relevant articles and documents
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Shorr
, p. 1390 (1954)
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One-Step Synthesis of Siloxanes from the Direct Process Disilane Residue
Neumeyer, Felix,Auner, Norbert
supporting information, p. 17165 - 17168 (2016/11/23)
The well-established Müller–Rochow Direct Process for the chloromethylsilane synthesis produces a disilane residue (DPR) consisting of compounds MenSi2Cl6?n(n=1–6) in thousands of tons annually. Technologically, much effort is made to retransfer the disilanes into monosilanes suitable for introduction into the siloxane production chain for increase in economic value. Here, we report on a single step reaction to directly form cyclic, linear, and cage-like siloxanes upon treatment of the DPR with a 5 m HCl in Et2O solution at about 120 °C for 60 h. For simplification of the Si?Si bond cleavage and aiming on product selectivity the grade of methylation at the silicon backbone is increased to n≥4. Moreover, the HCl/Et2O reagent is also suitable to produce siloxanes from the corresponding monosilanes under comparable conditions.
Improved Procedure for the Selective Reduction of Carbonyl Compounds and Carboxylic Acid Esters by Potassium Salt-Induced Hydrosilylation
Chuit, C.,Corriu, R. J. P.,Perz, R.,Reye, C.
, p. 981 - 984 (2007/10/02)
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