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β-(Cyclohexylamino)-crotonsaeure-methylester, also known as methyl β-(cyclohexylamino)crotonate, is an organic compound with the chemical formula C11H19NO2. It is a colorless to pale yellow liquid with a molecular weight of 197.27 g/mol. β-(Cyclohexylamino)-crotonsaeure-methylester is characterized by the presence of a cyclohexylamine group attached to a crotonic acid ester moiety, which is a methyl ester in this case. It is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of certain pesticides and drugs. The compound is known for its reactivity and can participate in various chemical reactions, such as Michael additions and condensations, making it a valuable building block in organic synthesis.

60913-92-0

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60913-92-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60913-92-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,9,1 and 3 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 60913-92:
(7*6)+(6*0)+(5*9)+(4*1)+(3*3)+(2*9)+(1*2)=120
120 % 10 = 0
So 60913-92-0 is a valid CAS Registry Number.

60913-92-0Downstream Products

60913-92-0Relevant academic research and scientific papers

Synthesis of Indoles and Pyrroles Utilizing Iridium Carbenes Generated from Sulfoxonium Ylides

Vaitla, Janakiram,Bayer, Annette,Hopmann, Kathrin H.

, p. 4277 - 4281 (2017)

Metal carbenes can undergo a myriad of synthetic transformations. Sulfur ylides are potential safe precursors of metal carbenes. Herein, we report cascade reactions that involve carbenoids derived from sulfoxonium ylides for the efficient and regioselective synthesis of indoles and pyrroles. The tandem action of iridium and Br?nsted acid catalysts enables rapid assembly of the heterocycles from unmodified anilines or readily accessible enamines under microwave irradiation. The key mechanistic steps are the catalytic transformation of the sulfoxonium ylide into an iridium–carbene complex, followed by N?H or C?H functionalization of an aniline or enamine, respectively, and a final acid-catalyzed cyclization. The present method was successfully applied to the synthesis of the densely functionalized pyrrole subunit of atorvastatin.

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