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19862-91-0

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19862-91-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 19862-91-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,8,6 and 2 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 19862-91:
(7*1)+(6*9)+(5*8)+(4*6)+(3*2)+(2*9)+(1*1)=150
150 % 10 = 0
So 19862-91-0 is a valid CAS Registry Number.

19862-91-0Relevant articles and documents

Polymer-bound chiroptical molecular switches; photochemical modification of the chirality of thin films

Oosterling, Michiel L.C.M.,Schoevaars, Anne Marie,Haitjema, Henk J.,Feringa, Ben L.

, p. 341 - 348 (1996)

Photobistable chiral polymers were obtained by covalent attachment of inherently dissymmetric 2-hydroxy-9-(7′methyl-1′,2′,3′,4′- tetrahydrophenanthrene-4′-ylidene)-9H-thioxanthene to methacrylate copolymers with appropriate spacers. Upon irradiation at 300 nm the optical activity of thin films of these polymers could be altered.

Transition-metal-free synthesis of unsymmetrical diaryl chalcogenides from arenes and diaryl dichalcogenides

Prasad, Ch Durga,Balkrishna, Shah Jaimin,Kumar, Amit,Bhakuni, Bhagat Singh,Shrimali, Kaustubh,Biswas, Soumava,Kumar, Sangit

, p. 1434 - 1443 (2013/03/29)

A transition-metal-free synthetic method has been developed for the synthesis of unsymmetrical diaryl chalcogenides (S, Se, and Te) from diaryl dichalcogenides and arenes under oxidative conditions by using potassium persulfate at room temperature. Variously substituted arenes such as anisole, thioanisole, diphenyl ether, phenol, naphthol, di- and trimethoxy benzenes, xylene, mesitylene, N,N-dimethylaniline, bromine-substituted arenes, naphthalene, and diaryl dichalcogenides underwent carbon-chalcogen bond-forming reaction to give unsymmetrical diaryl chalcogenides in trifluoroacetic acid. To understand the mechanistic part of the reaction, a detailed in situ characterization of the intermediates has been carried out by 77Se NMR spectroscopy by using diphenyl diselenide as the substrate. 77Se NMR study suggests that electrophilic species ArE+ is generated by the reaction of diaryl dichalcogenide with persulfate in trifluoroacetic acid. The electrophilic attack of arylchalcogenium ion on the arene may be responsible for the formation of the aryl-chalcogen bond.

Design, synthesis, biological evaluation, and NMR studies of a new series of arylsulfones as selective and potent matrix metalloproteinase-12 inhibitors

Nuti, Elisa,Panelli, Laura,Casalini, Francesca,Avramova, Stanislava I.,Orlandini, Elisabetta,Santamaria, Salvatore,Nencetti, Susanna,Tuccinardi, Tiziano,Martinelli, Adriano,Cercignani, Giovanni,D'Amelio, Nicola,Maiocchi, Alessandro,Uggeri, Fulvio,Rossello, Armando

experimental part, p. 6347 - 6361 (2010/03/24)

Overexpression of macrophage elastase (MMP-12), a member of the matrix metalloproteinases family, can be linked to tissue remodeling and degradation in some inflammatory processes, such as chronic obstructive pulmonary disease (COPD), emphysema, rheumatoi

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