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What is the DIETHYL(TRIMETHYLSILYLMETHYL)MALONATE ?
DIETHYL(TRIMETHYLSILYLMETHYL)MALONATE is , while it's Molecular Formula is C11H22 O4 Si. Used in Organic Synthesis:
DIETHYL(TRIMETHYLSILYLMETHYL)MALONATE is used as a reagent for the synthesis of various organic compounds due to its trimethylsilyl-protected methyl group, which facilitates the formation of carbon-carbon bonds and the creation of complex molecular structures.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, DIETHYL(TRIMETHYLSILYLMETHYL)MALONATE is utilized as a building block for the synthesis of complex molecules with potential therapeutic applications, contributing to the development of new drugs.
Used in Agricultural Industry:
Similarly, in agriculture, DIETHYL(TRIMETHYLSILYLMETHYL)MALONATE is employed in the synthesis of molecules with pesticidal or herbicidal properties, thereby aiding in the production of more effective crop protection agents.
Used as a Cross-Coupling Reagent:
DIETHYL(TRIMETHYLSILYLMETHYL)MALONATE is also used as a cross-coupling reagent in organic reactions, particularly for the formation of carbon-carbon bonds, which is crucial in assembling larger and more complex organic molecules.
What is the CAS number for DIETHYL(TRIMETHYLSILYLMETHYL)MALONATE ?
The CAS number of DIETHYL(TRIMETHYLSILYLMETHYL)MALONATE is 17962-38-8.
More information of DIETHYL(TRIMETHYLSILYLMETHYL)MALONATE 17962-38-8 are:
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Synonyms |
Malonicacid, [(trimethylsilyl)methyl]-, diethyl ester (6CI,8CI); Propanedioic acid,[(trimethylsilyl)methyl]-, diethyl ester (9CI); Diethyl2-(trimethylsilylmethyl)malonate |
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CAS?Number |
17962-38-8 |
|
Molecular Formula |
C11H22 O4 Si |
|
Molecular Weight |
246.379 |
|
Density |
0.973 g/cm3 |
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Boiling Point |
252.8 °C at 760 mmHg |
|
Flash Point |
88.7 °C |
|
HS CODE |
2931900090 |
|
PSA |
52.60000 |
|
LogP |
2.06700 |
What is DIETHYL(TRIMETHYLSILYLMETHYL)MALONATE (17962-38-8) used for?
DIETHYL(TRIMETHYLSILYLMETHYL)MALONATE, a chemical compound with the molecular formula C12H26O4Si, is a colorless liquid characterized by a fruity odor. It is a derivative of malonic acid, featuring a trimethylsilyl-protected methyl group, which renders it a valuable precursor for the synthesis of a variety of organic compounds. DIETHYL(TRIMETHYLSILYLMETHYL)MALONATE is also recognized for its utility as a cross-coupling reagent in organic reactions, especially in the formation of carbon-carbon bonds. Its applications extend to the construction of complex molecules with relevance in pharmaceutical and agricultural sectors, establishing DIETHYL(TRIMETHYLSILYLMETHYL)MALONATE as a versatile and significant chemical in organic chemistry.
InChI:InChI=1/C7H10N2/c1-2-3-7-6-8-4-5-9-7/h4-6H,2-3H2,1H3
Articles related to DIETHYL(TRIMETHYLSILYLMETHYL)MALONATE:
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Article |
Source |
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Synthesis of rac-2′-(trimethylsilyl)isovaline: A novel silicon-containing α,α-dialkylated α-amino acid |
Falgner, Steffen,Buchner, Ginka,Tacke, Reinhold , p. 2614 - 2617 (2010) |
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2-ALKOXYCARBONYLALLYLTRIMETHYLSILANES AS NEW REAGENTS OF 2-ALKOXYCARBONYLALLYLATION OF ELECTROPHILES |
Hosomi, Akira,Hashimoto, Hidehiko,Sakurai, Hideki , p. 951 - 954 (2007/10/02) |
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