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4'-O-trimethylsilylacetovanillone is a chemical compound with the molecular formula C11H14O2Si. It is a derivative of acetovanillone, where a trimethylsilyl group (Si(CH3)3) is attached to the 4'-hydroxyl group of the molecule. This modification can enhance the stability and reactivity of the compound in various chemical reactions. The trimethylsilyl group is known for its ability to protect hydroxyl groups and can be easily removed under mild conditions, making 4'-O-trimethylsilylacetovanillone a valuable intermediate in organic synthesis. It is used in the preparation of various pharmaceuticals and other organic compounds that require a protected phenolic group.

6689-44-7

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6689-44-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6689-44-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,8 and 9 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6689-44:
(6*6)+(5*6)+(4*8)+(3*9)+(2*4)+(1*4)=137
137 % 10 = 7
So 6689-44-7 is a valid CAS Registry Number.

6689-44-7Downstream Products

6689-44-7Relevant academic research and scientific papers

29Si and 13C NMR Spectra of 4-Substituted 2-Methoxytrimethylsiloxybenzenes. Factors Determining the Chemical Shifts in Models of Lignin Constituents

Schraml, Jan,Kvicalova, Magdalena,Chvalovsky, Vaclav,Elder, Thomas,Brezny, Robert

, p. 973 - 978 (2007/10/02)

29Si and 13C NMR chemical shifts are reported for a series of twenty 4-substituted 2-methoxytrimethylsiloxybenzenes; the set of substituents incorporates a basic set of ten substituents differing in their relative polar and resonance effects and ten other

PHENOLIC COMPOUNDS FROM ROOTS OF URTICA DIOICA

Kraus, Rupert,Spiteller, Gerhard

, p. 1653 - 1659 (2007/10/02)

Root extracts from Urtica dioica were separated into several classes of compounds by extraction with organic solvents at different pH values.The phenolic fraction was analysed by GC-MS after trimethylsilylation.This procedure allowed the identification of 18 phenolic compounds as well as the detection of eight lignans.The occurrence of some of these substances in this plant was previously unknown.

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