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(4S,5S)-4-benzyl-N-(benzyloxycarbonyl)-5-(trifluoromethyl)-5-[(trimethylsilyl)oxy]-1,3-oxazolidine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

191981-04-1

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191981-04-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 191981-04-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,1,9,8 and 1 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 191981-04:
(8*1)+(7*9)+(6*1)+(5*9)+(4*8)+(3*1)+(2*0)+(1*4)=161
161 % 10 = 1
So 191981-04-1 is a valid CAS Registry Number.

191981-04-1Downstream Products

191981-04-1Relevant academic research and scientific papers

Solkane 365mfc is an environmentally benign alternative solvent for trifluoromethylation reactions

Kusuda, Akihiro,Kawai, Hiroyuki,Nakamura, Shuichi,Shibata, Norio

supporting information; experimental part, p. 1733 - 1735 (2011/03/19)

Solkane 365mfc is introduced for the first time as a new, environmentally benign alternative solvent for nucleophilic trifluoromethylation reactions. The Royal Society of Chemistry 2009.

Reaction of (Trifluoromethyl)trimethylsilane with Oxazolidin-5-ones: Synthesis of Peptidic and Nonpeptidic Trifluoromethyl Ketones

Walter, Magnus W.,Adlington, Robert M.,Baldwin, Jack E.,Schofield, Christopher J.

, p. 5179 - 5192 (2007/10/03)

(Trifluoromethyl)trimethylsilane (TMS-CF3, the Ruppert Reagent) reacts with a variety of amino acid derived N-substituted oxazolidin-5-ones in excellent yields. Mild acid hydrolysis of adducts with electron-releasing substituents at C-2 affords

Reaction of ruppert's reagent (TMS-CF3) with Oxazolidinones: Synthesis of protected α-amino trifluoromethylketones

Walter, Magnus W.,Adlington, Robert M.,Baldwin, Jack E.,Chuhan, John,Schofield, Christopher J.

, p. 7761 - 7764 (2007/10/02)

(Trifluoromethyl)trimethylsilane adds to α-amino acid derived oxazolidin-5-ones in excellent yields. The adducts can be converted into protected α-amino trifluoromethylketones by acid hydrolysis.

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