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Methanone, 3-furanyl(4-methoxyphenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

68204-87-5

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68204-87-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 68204-87-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,2,0 and 4 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 68204-87:
(7*6)+(6*8)+(5*2)+(4*0)+(3*4)+(2*8)+(1*7)=135
135 % 10 = 5
So 68204-87-5 is a valid CAS Registry Number.

68204-87-5Relevant academic research and scientific papers

Ni-Catalyzed cross-coupling reactions of N-acylpyrrole-type amides with organoboron reagents

Huang, Pei-Qiang,Chen, Hang

supporting information, p. 12584 - 12587 (2017/11/30)

The catalytic conversion of amides to ketones is highly desirable yet challenging in organic synthesis. We herein report the first Ni/bis-NHC-catalyzed cross-coupling of N-acylpyrrole-type amides with arylboronic esters to obtain diarylketones. This method is facilitated by a new chelating bis-NHC ligand. The reaction tolerates diverse functional groups on both arylamide and arylboronic ester partners including sensitive ester and ketone groups.

Palladium-Catalyzed Cross-Carbonylation of Aryl Iodides with Five-Membered Cyclic Olefins

Satoh, Tetsuya,Itaya, Tomoaki,Okuro, Kazumi,Miura, Masahiro,Nomura, Masakatsu

, p. 7267 - 7271 (2007/10/03)

Intermolecular cross-carbonylation of aryl iodides with five-membered cyclic olefins such as dihydrofurans and cyclopentene was found to proceed by using a catalyst system of PdCl2/PPh3 under CO (3-5 atm) in the presence of a tertiary amine.With 2,3- and 2,5-dihydrofurans, 2-aroyl-4,5-dihydro- and 3-aroyl-2,3-dihydrofurans were obtained as the predominant products, respectively, while the reaction of iodobenzene with cyclopentene gave a mixture of three regioisomers of benzoylcyclopentene.The yields of the products were observed to be markedly influenced by the amount of triphenylphosphine added.

4-Substituted thiophene- and furan-2-sulfonamides as topical carbonic anhydrase inhibitors

Hartman,Halczenko,Smith,Sugrue,Mallorga,Michelson,Randall,Schwam,Sondey

, p. 3822 - 3831 (2007/10/02)

A series of 4-substituted thiophene- and furan-2-sulfonamides was prepared and was found to possess nanomolar-level potency for inhibition of human carbonic anhydrase II in vitro. Selected examples from this group were further evaluated for their potentia

4-(benzoyl)thiophene(or furan)-sulfonamide and derivatives thereof for the topical treatment of elevated intraocular pressures

-

, (2008/06/13)

4-(benzoyl)thiophene(or furan)-2-sulfonamide and derivatives thereof are useful for the topical treatment of elevated intraocular pressure.

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