43112-38-5 Usage
Description
3-Trimethylsilyl-2-oxazolidinone is an organic compound characterized by a five-membered oxazolidinone ring with a trimethylsilyl group attached to the 3-position. This unique structure endows it with specific chemical properties that make it a versatile reagent in various applications.
Uses
Used in Chemical Synthesis:
3-Trimethylsilyl-2-oxazolidinone is used as a salivating agent for the silylation of carboxylic acids, 1,3-dicarbonyl compounds, and hydroxyl compounds. The silylation process involves the conversion of these functional groups into their corresponding trimethylsilyl ethers, which can be beneficial for protecting these groups during chemical reactions or for enhancing their reactivity under certain conditions.
Used in Pharmaceutical Industry:
3-Trimethylsilyl-2-oxazolidinone is utilized as a pharmaceutical intermediate. In this context, it serves as a key building block or a precursor in the synthesis of various pharmaceutical compounds. Its unique structure and reactivity can be harnessed to create new drugs or improve the synthesis processes of existing ones, potentially leading to more effective medications or more efficient production methods.
Check Digit Verification of cas no
The CAS Registry Mumber 43112-38-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,3,1,1 and 2 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 43112-38:
(7*4)+(6*3)+(5*1)+(4*1)+(3*2)+(2*3)+(1*8)=75
75 % 10 = 5
So 43112-38-5 is a valid CAS Registry Number.
InChI:InChI=1/C6H13NO2Si/c1-10(2,3)7-4-5-9-6(7)8/h4-5H2,1-3H3
43112-38-5Relevant articles and documents
TRIMETHYLSILYL TRICHLOROACETATE: A NEW REAGENT FOR SALT-FREE SILYLATIONS
Renga, James M.,Pen-Chung, Wang
, p. 1175 - 1178 (2007/10/02)
Trimethylsylil trichloroacetate (1) is a convenient reagent for the silylation of phenols, carboxylic acids, mercaptans, amides, acetylenes, and β-keto esters, while the reaction of 1 with aldehydes and ketones affords silylated trichloromethyl carbinols (5).
A Convenient Synthesis of Trimethylsilyl Carboxylates using N-Trimethylsilyl-2-oxazolidinone in the Absence of Catalysts
Palomo, C.
, p. 809 - 811 (2007/10/02)
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