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Cyclohexanone O-triethylsilyl oxime is a chemical compound derived from cyclohexanone, an organic ketone. It is formed by the reaction of cyclohexanone with hydroxylamine and triethylsilane, resulting in the formation of an oxime group attached to the carbonyl carbon of cyclohexanone. cyclohexanone O-triethylsilyl oxime is characterized by its molecular formula C12H25NOSi and a molar mass of 221.42 g/mol. It is a colorless liquid with a density of 0.84 g/cm3 and a boiling point of 90-92°C at 20 mmHg. Cyclohexanone O-triethylsilyl oxime is used as a protecting group in organic synthesis, particularly in the protection of carbonyl groups, and is also employed in the synthesis of various pharmaceuticals and agrochemicals.

7449-73-2

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7449-73-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7449-73-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,4 and 9 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 7449-73:
(6*7)+(5*4)+(4*4)+(3*9)+(2*7)+(1*3)=122
122 % 10 = 2
So 7449-73-2 is a valid CAS Registry Number.

7449-73-2Downstream Products

7449-73-2Relevant academic research and scientific papers

Pt-catalyzed O-silylation of oximes by tri-substituted organosilanes

Bhatt, Shreeja V.,Bhatt, Shreya V.,Fotie, Jean

supporting information, p. 1636 - 1639 (2019/06/04)

Silylated derivatives of oximes are important intermediates in organic synthesis, and have found application in the preparation of various nitrogen containing compounds including nitriles, amines, nitrones, and hydroxylamines. An efficient method for the

An efficient synthesis of silyl ethers of primary alcohols, secondary alcohols, phenols and oximes with a hydrosilane using InBr3 as a catalyst

Sridhar, Madabhushi,Raveendra, Jillella,China Ramanaiah, Beeram,Narsaiah, Chinthala

experimental part, p. 5980 - 5982 (2011/12/02)

An efficient method for the preparation of silyl ethers by InBr3 catalyzed silylation of primary alcohols, secondary alcohols, phenols and oxime with a hydrosilane is described.

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