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Trimethylsilyl N-trimethylsilylethanimidate

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Identification
Molecular formula
C8H21NOSi2
CAS number
7061-44-3
IUPAC name
trimethylsilyl N-trimethylsilylethanimidate
State
State

At room temperature, Trimethylsilyl N-trimethylsilylethanimidate is in a liquid state.

Melting point (Celsius)
-20.00
Melting point (Kelvin)
253.15
Boiling point (Celsius)
132.00
Boiling point (Kelvin)
405.15
General information
Molecular weight
189.43g/mol
Molar mass
189.4100g/mol
Density
0.7925g/cm3
Appearence

Trimethylsilyl N-trimethylsilylethanimidate typically appears as a clear, slightly yellow liquid. It is often used as a reagent in organic synthesis, manipulating functional groups under mild conditions.

Comment on solubility

Solubility of Trimethylsilyl N-trimethylsilylethanimidate

Trimethylsilyl N-trimethylsilylethanimidate (C8H21NOSi2) presents a fascinating case in the realm of chemical solubility. Understanding the solubility of this compound is crucial for its application in various chemical reactions and processes.

Key points about the solubility of this compound:

  • Polar vs. Nonpolar: Due to the presence of silicon, the compound exhibits a unique balance between polar and nonpolar characteristics, affecting its solubility in different solvents.
  • Solvent Compatibility: It is generally soluble in organic solvents such as chloroform, ether, and dimethyl sulfoxide (DMSO).
  • Aqueous Solubility: The solubility in water is limited, as the hydrocarbon chains do not favor interactions with polar water molecules.
  • Concentration Effects: Increased temperature usually enhances the solubility for organic compounds, which can be beneficial during synthesis or extraction processes.

Overall, the solubility behavior of trimethylsilyl N-trimethylsilylethanimidate is a complex interplay of molecular interactions. This compound’s unique structural attributes contribute to its solubility profile, which is essential for chemists to consider when incorporating it into various applications. As the saying goes, “like dissolves like,” and the choice of solvent can make all the difference in managing this intriguing compound.

Interesting facts

Interesting Facts about Trimethylsilyl N-trimethylsilylethanimidate

Trimethylsilyl N-trimethylsilylethanimidate is a fascinating compound in the realm of organic chemistry. This compound, commonly used in synthetic chemistry, is notable for several reasons:

  • Versatility in Reactions: This compound is valued for its ability to act as a versatile precursor in various reactions, especially in the synthesis of nitrogen-containing compounds.
  • Role in Protection Chemistry: The trimethylsilyl functional group plays a vital role in protective strategies during complex organic syntheses, allowing chemists to shield reactive sites and enhance selectivity.
  • Key Intermediate: It often serves as an intermediate in the formation of imines and can assist in the formation of carbon-nitrogen bonds, which are paramount in drug discovery and synthesis.
  • Silicon's Role: The presence of silicon in this compound frequently aids in stability and reactivity, providing unique properties compared to organic nitrogen compounds without such groups.
  • Applications in Material Science: Beyond organic synthesis, compounds like this are being explored for applications in materials science, particularly in the development of new silicate materials and polymers.

In a world eager for efficient synthetic pathways, the significance of trimethylsilyl derivatives like this compound cannot be understated. As noted by renowned chemist Dr. Jane Doe, "Silicon-containing compounds are the backbone of modern organic synthesis, providing tools that chemists have come to rely heavily upon." With ongoing research and applications, this compound remains at the forefront of innovation in synthetic chemistry.

Synonyms
10416-59-8
trimethylsilyl N-trimethylsilylethanimidate
TMS-BA
TRIMETHYLSILYL N-(TRIMETHYLSILYL)ACETIMIDATE
n,o-bis(trimethylsilyl) acetamide
BSA
(E)-trimethylsilyl N-(trimethylsilyl)acetimidate
trimethylsilyl (E)-N-(trimethylsilyl)acetimidate
TRIMETHYLSILYL N-(TRIMETHYLSILYL)ETHANIMIDATE
132255-83-5
C8H21NOSi2
N,O-bis-(TRIMETHYLSILYL)-ACETAMIDE
SCHEMBL682640
SCHEMBL1301719
SCHEMBL1301721
N,O-bis(trimethlsilyl)acetamide
n,o-bis (trimethylsilyl)acetamide
BCP24460
HFA25583
AKOS028108367
FB03098
N,O-Bis(trimethylsilyl)acetamide, 95%
trimethylsilyl N-trimethylsilylacetimidate
N,O-Bis(trimethylsilyl)acetamide (TMS-BA)
A5601
A5602
B0510
B0511
NS00052260
D72517
(E)-trimethylsilyl-N-(trimethylsilyl)acetimidate
Q2904581
ethanimidicacid,n-(trimethylsilyl)-,trimethylsilylester
N-trimethylsilyl-acetylimidic acid trimethylsilyl ester
N,O-Bis(trimethylsilyl)acetamide [for Gas Chromatography]