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dimethyl 2-cinnamyl-2-(prop-2-yn-1-yl)malonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

130860-69-4

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130860-69-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 130860-69-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,8,6 and 0 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 130860-69:
(8*1)+(7*3)+(6*0)+(5*8)+(4*6)+(3*0)+(2*6)+(1*9)=114
114 % 10 = 4
So 130860-69-4 is a valid CAS Registry Number.

130860-69-4Relevant academic research and scientific papers

Ruthenium catalyzed enyne cycloisomerizations and hydroxycyclizations with skeletal rearrangement

Faller,Fontaine, Philip P.

, p. 1912 - 1918 (2006)

A neutral arene-tethered ruthenium complex was found to be a catalyst precursor for enyne cycloisomerizations and hydroxycyclizations. The observed products were the result of a skeletal rearrangement process, and include an unusual cyclization to form a six-membered ring. Labeling studies on the six-membered ring product are in accord with an electrophilic activation mechanism that proceeds via cationic cyclopropyl carbene intermediates.

Complementary Reactivity of 1,6-Enynes with All-Metal Aromatic Trinuclear Complexes and Carboxylic Acids

Cecchini, Chiara,Lanzi, Matteo,Cera, Gianpiero,Malacria, Max,Maestri, Giovanni

supporting information, p. 1216 - 1224 (2019/02/26)

The distinct reactivity of 1,6-enynes in the presence of a trinuclear metal complex activated by a carboxylic acid is presented. The triplatinum catalyst enables the cyclization of the substrate and subsequent incorporation of a nucleophile in the final product. In contrast, sequential cyclization/double bond shift occurs under analogous conditions in the presence of the corresponding tripalladium complex.

Diastereoselective cycloisomerizations of enediynes via palladium catalysis

Trost,Shi

, p. 12491 - 12509 (2007/10/02)

Considerations of atom economy drive a search for reactions that are simple additions which, performed intramolecularly, are cycloisomerizations. Exposure of acyclic enediynes to a catalyst generated by mixing a Pd(0) complex with acetic acid normally in

Ligand dependence of molybdenum-catalyzed alkylations. Molybdenum-isonitrile complexes as a new class of highly reactive alkylation catalysts

Trost, Barry M.,Merlic, Craig A.

, p. 9590 - 9600 (2007/10/02)

A series of molybdenum complexes bearing α-diimine, N,N′-diarylideneethylenediamine, and isonitrile ligands have been prepared and evaluated for their ability to catalyze alkylations by using allyl acetates and especially allyl sulfones. (bpy)Mo(CH3

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