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2-phenyl-1-oxa-spiro[4.4]non-2-en-4-one is a complex organic chemical compound characterized by a unique spirocycle structure. It features a phenyl group attached to a spiro ring system, which consists of a four-membered oxacycle (a ring containing an oxygen atom) fused to a four-membered carbon cycle. The molecule has a carbonyl group at the 4-position, which contributes to its reactivity and potential applications in organic synthesis. 2-phenyl-1-oxa-spiro[4.4]non-2-en-4-one may be of interest in the development of pharmaceuticals, agrochemicals, or other specialty chemicals due to its structural diversity and the possibility of functional group manipulation.

5198-67-4

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5198-67-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5198-67-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,1,9 and 8 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5198-67:
(6*5)+(5*1)+(4*9)+(3*8)+(2*6)+(1*7)=114
114 % 10 = 4
So 5198-67-4 is a valid CAS Registry Number.

5198-67-4Downstream Products

5198-67-4Relevant academic research and scientific papers

Silver-free activation of ligated gold(I) chlorides: The use of [Me3NB12Cl11]- as a weakly coordinating anion in homogeneous gold catalysis

Wegener, Michael,Huber, Florian,Bolli, Christoph,Jenne, Carsten,Kirsch, Stefan F.

supporting information, p. 1328 - 1336 (2015/02/05)

Phosphane and N-heterocyclic carbene ligated gold(I) chlorides can be effectively activated by Na[Me3NB12Cl11] (1) under silver-free conditions. This activation method with a weakly coordinating closo-dodecaborate anion was shown to be suitable for a large variety of reactions known to be catalyzed by homogeneous gold species, ranging from carbocyclizations to heterocyclizations. Additionally, the capability of 1 in a previously unknown conversion of 5-silyloxy-1,6-allenynes was demonstrated.

Reactivity of 3-silyloxy-1,4-enynes: Gold(III)-catalyzed regioselective nucleophilic substitution

Haug, Timm T.,Harschneck, Tobias,Duschek, Alexander,Lee, Chang-Uk,Binder, J?rg T.,Menz, Helge,Kirsch, Stefan F.

scheme or table, p. 510 - 514 (2009/06/05)

Gold-catalyzed reactions of 3-silyloxy-1,4-enynes with alcohols afford primary, secondary, and tertiary pent-2-en-4-ynyl ethers in moderate to excellent yields. The substitution proceeds with high regioselectivity. An initial cyclization providing five-me

Pt-catalyzed cyclization/migration of propargylic alcohols for the synthesis of 3(2H)-furanones, pyrrolones, indolizines, and indolizinones

Bunnelle, Eric M.,Smith, Cameron R.,Lee, Sharon K.,Singaram, Surendra W.,Rhodes, Allison J.,Sarpong, Richmond

, p. 7008 - 7014 (2008/09/21)

Several heterocycles such as furanones, pyrrolones, and indolizines, which are of pharmacological importance, are easily accessed via the Pt(II)-catalyzed heterocyclization/1,2-migration of propargylic ketols or hydroxy imine derivatives. This method sidesteps the challenges of traditional heteroaromatic oxygenation strategies such as regioselectivity and functional group tolerance in the syntheses of these heterocycles.

Synthesis of heterocyclic systems by transition-metal-catalyzed cyclization-migration reactions - A diversity-oriented strategy for the construction of spirocyclic 3(2H)-furanones and 3-pyrrolones

Binder, Joerg T.,Crone, Benedikt,Kirsch, Stefan F.,Liebert, Clemence,Menz, Helge

, p. 1636 - 1647 (2008/02/06)

Two platinum(II)-catalyzed heterocyclization-migration reactions that provide five-membered heterocycle products are described. With 5 mol-% of PtCl2 as a catalyst, 2-alkynyl-2-hydroxy carbonyl compounds 1 are converted into 3(2H)-furanones 2 a

Gold(III)- and platinum(II)-catalyzed domino reaction consisting of heterocyclization and 1,2-migration: Efficient synthesis of highly substituted 3(2H)-furanones

Kirsch, Stefan F.,Binder, Joerg T.,Liebert, Clemence,Menz, Helge

, p. 5878 - 5880 (2007/10/03)

(Chemical Equation Presented) PtCl2-catalyzed alkyne activation initiates a domino reaction, in which a heterocyclization is followed by a 1,2-alkyl migration, for the construction of a variety of substituted 3(2H)-furanones. This stereospecifi

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