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3-ethoxy-6-(2-butynyl)-cyclohex-2-en-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

99196-38-0

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99196-38-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 99196-38-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,1,9 and 6 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 99196-38:
(7*9)+(6*9)+(5*1)+(4*9)+(3*6)+(2*3)+(1*8)=190
190 % 10 = 0
So 99196-38-0 is a valid CAS Registry Number.

99196-38-0Relevant academic research and scientific papers

Copper-catalyzed vinylsilane allylation

Cornelissen, Loic,Vercruysse, Sebastien,Sanhadji, Ayoub,Riant, Olivier

, p. 35 - 38 (2014)

Soft reaction conditions, particularly important in total synthesis, have dragged many researchers into the field of silylated organic compounds. Hereby, we describe a new copper-catalyzed vinylsilane transformation. Various vinylsilanes were allylated by using a copper(I) salt, and this led to the formation of polysubstituted 1,4-dienes bearing sensitive moieties such as halogens, ketones, and aldehydes. Hereby is described a new copper-catalyzed vinylsilane transformation. Various vinylsilanes were allylated by using copper(I) salts, and this led to the formation of polysubstituted 1,4-dienes bearing sensitive moieties such as halogens, ketones, and aldehydes. TBAT = tetrabutylammonium difluorotriphenylsilicate. Copyright

Reductive cyclization of α-cyclopropylketones with alkynyl- and aryl- tethered substituents

Fagnoni, Maurizio,Schmoldt, Philip,Kirschberg, Thorsten,Mattay, Jochen

, p. 6427 - 6444 (2007/10/03)

Photoinduced electron transfer (PET) reactions of α-cyclopropyl- substituted ketones and triethylamine (TEA) were used to initiate the cyclopropylcarbinyl-homoallyl rearrangement. The intramolecular cyclization reaction onto triple bonds was performed yielding bicyclic and spirocyclic compounds. Furthermore, in some preliminary studies it was shown that even intramolecular aromatic substitutions are feasible.

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