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2-(2-bromophenyl)-2-methyl-1,3-dithiane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

219606-57-2

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219606-57-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 219606-57-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,9,6,0 and 6 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 219606-57:
(8*2)+(7*1)+(6*9)+(5*6)+(4*0)+(3*6)+(2*5)+(1*7)=142
142 % 10 = 2
So 219606-57-2 is a valid CAS Registry Number.

219606-57-2Relevant academic research and scientific papers

Alcohol-mediated direct dithioacetalization of alkynes with 2-chloro-1,3-dithiane for the synthesis of Markovnikov dithianes

Liu, Teng,Tian, Lixia,Lai, Junshan,Min, Deng,Qu, Mengnan,Tang, Shouchu

supporting information, p. 4068 - 4071 (2017/07/10)

An alcohol-mediated dithioacetalization process that gains direct access to the corresponding Markovnikov-selective 1,3-dithianes using unactivated alkynes and nonthiolic/odorless 2-chloro-1,3-dithiane in a highly efficient manner has been developed. This methodology has the advantage of having mild reaction conditions, and the dithioacetalization process gives good to excellent yields with high Markovnikov-selectivity.

Intramolecularly sulfur-stabilized silicon cations as Lewis acid catalysts

Rohde, Volker H. G.,Pommerening, Phillip,Klare, Hendrik F. T.,Oestreich, Martin

, p. 3618 - 3628 (2014/08/05)

The synthesis and spectroscopic characterization of previously unprecedented sulfur-stabilized silicon cations are reported. Several 1,3-dithiolan-2-yl- and 1,3-dithian-2-yl-substituted silanes were prepared and successfully transformed into the corresponding silicon cations by hydride abstraction. The silicon-sulfur interaction creates three consecutive stereocenters at three different elements. It is remarkable that the present stereocenter at the silicon atom determines the stereochemical outcome at the formerly prochiral sulfur and carbon atoms with excellent diastereoselectivity. All sulfur-stabilized silicon cations are shown to be potent catalysts in a challenging Diels-Alder reaction. Moreover, structurally related oxazoline-stabilized silicon cations were generated and characterized but found to be unreactive.

Sulfur as a bridge: Synthesis of medium rings via a bicyclic sulfonium ion

Zhou, Hongwei,Xing, Yanpeng,Liu, Le,Hong, Junjie

scheme or table, p. 3146 - 3150 (2012/01/02)

A facile and efficient synthesis of medium rings via a bicyclic sulfonium ion was developed. Spectroscopic evidence for the formation of an intermediate sulfonium moiety is provided. The sulfur atom served as a "bridge" to access the medium ring system and could be removed after use via a Ramberg-Baecklund process. As a result of the readily available starting materials, simple operation, and mild conditions, these reactions should be an appealing strategy in organic synthesis. Copyright

2,3-Dihydro-dithiin and -dithiepine-1,1,4,4-tetroxides: Small molecule non-peptide antagonists of the human galanin hGAL-1 receptor

Scott, Malcolm K.,Ross, Tina M.,Lee, Daniel H. S.,Wang, Hoau-Yan,Shank, Richard P.,Wild, Kenneth D.,Davis, Coralie B.,Crooke, Jeffrey J.,Potocki, Alexander C.,Reitz, Allen B.

, p. 1383 - 1391 (2007/10/03)

The neuropeptide galanin modulates several physiological functions such as cognition, learning, feeding behavior, and depression, probably via the galanin 1 receptor (GAL-R1). Using an HTS assay based on 125I-human galanin binding to the human

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