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22768-79-2

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22768-79-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 22768-79-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,7,6 and 8 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 22768-79:
(7*2)+(6*2)+(5*7)+(4*6)+(3*8)+(2*7)+(1*9)=132
132 % 10 = 2
So 22768-79-2 is a valid CAS Registry Number.

22768-79-2Downstream Products

22768-79-2Relevant articles and documents

Highly selective 30% hydrogen peroxide oxidation of sulfides to sulfoxides using micromixing

Noguchi, Takuya,Hirai, Yoshiro,Kirihara, Masayuki

, p. 3040 - 3042 (2008)

The highly selective oxidation of sulfides to sulfoxides using 30% hydrogen peroxide has been achieved under catalyst-free conditions using a T-shaped micromixer. The Royal Society of Chemistry.

Palladium-catalyzed suzuki-miyaura reaction involving a secondary sp 3 carbon: Studies of stereochemistry and scope of the reaction

Rodriguez, Nuria,De Arellano, Carmen Ramirez,Asensio, Gregorio,Medio-Simon, Mercedes

, p. 4223 - 4229 (2008/02/08)

Palladium-catalyzed C-C bond formation involving secondary sp 3-hybridized carbon is described. These reactions occur with secondary 1-bromoethyl arylsulfoxides and different arylboronic acids, to produce the corresponding arylated sulfoxides in moderate to high yields and with complete stereospecificity. Despite the presence of β hydrogens in the substrate, the competitive β-hydride elimination is not a significant side reaction when coordinating solvents are used. The reported cross-coupling involves secondary Csp3-Csp2 bond formation: this is the first time that a mechanistic study has been carried out with such substrates. The reaction proceeds with inversion of configuration at the stereogenic C sp3 carbon. The high stereospecificity of the coupling and the mildness of the reaction conditions allow for the preservation of the optical purities of reagents and products and the preparation of useful chiral targets.

Contrasting Pathways for the Directed Homogeneous Hydrogenation of Vinyl Sulfoxides and Vinyl Sulfones

Ando, David,Bevan, Christopher,Brown, John M.,Price, David W.

, p. 592 - 594 (2007/10/02)

Rh-complex catalysed directed hydrogenation of (α-hydroxyalkyl)vinyl sulfones follows the same stereochemical course as the corresponding acrylates, via HO-coordination; hydrogenation of the related (α-hydroxyalkyl)vinyl sulfoxides is directed by S-O coor

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