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(4S)-4-[(tert-Butyldimethylsilyl)oxy]-2-iodocyclohex-2-en-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

198407-83-9

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198407-83-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 198407-83-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,8,4,0 and 7 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 198407-83:
(8*1)+(7*9)+(6*8)+(5*4)+(4*0)+(3*7)+(2*8)+(1*3)=179
179 % 10 = 9
So 198407-83-9 is a valid CAS Registry Number.

198407-83-9Relevant academic research and scientific papers

A convergent synthesis of the tricyclic core of the dictyosphaeric acids

Barfoot, Christopher W.,Burns, Alan R.,Edwards, Michael G.,Kenworthy, Martin N.,Ahmed, Mahmood,Shanahan, Stephen E.,Taylor, Richard J. K.

, p. 353 - 356 (2008/09/19)

(Chemical Equation Presented) The first synthetic route to the tricyclic core of the dictyosphaeric acids has been established starting from readily available (S)-(-)-4-(tert-butyldimethylsilyloxy)cyclohexenone and involving 9 steps, including a ring-clos

Approaches to the synthesis of (+)- and (-)-epibatidine

Barros, M. Teresa,Maycock, Christopher D.,Ventura, M. Rita

, p. 166 - 173 (2007/10/03)

Synthetic approaches to the powerful analgesic alkaloids (+)- and (-)-epibatidine are described. The starting material employed was natural (-)-quinic acid from which chiral enones and α-iodoenones were prepared. Stille coupling afforded suitable substrat

The effect of DMSO on the borohydride reduction of a cyclohexanone: A formal enantioselective synthesis of (+)-epibatidine

Barros, M. Teresa,Maycock, Christopher D.,Ventura, M. Rita

, p. 557 - 560 (2007/10/03)

An asymmetric synthesis of (+)-epibatidine is described which uses the increased stereoselectivity of a borohydride reduction induced by the presence of DMSO.

First generation of the dienediyne portion of a dienediyne model of the neocarzinostatin chromophore by a McMurry reaction

Rucker, Mark,Brueckner, Reinhard

, p. 7353 - 7356 (2007/10/03)

The first 3→6 type ring-closing dienediyne synthesis by means of a McMurry reaction was realized by converting the ketoaldehyde 20 into the 6-/10-membered bicyclic dienediyne 22. Diastereoselective pinacol couplings 20→23 and 21→24 giving 6-/10-membered b

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