22308-11-8

Upstream product

• 2658-60-8 1,1-bis(hydroxymethyl)cyclohexane 
• 98-59-9 p-toluenesulfonyl chloride 
• 1139-13-5 diethyl cyclohexane-1,1-dicarboxylate 
• 111-24-0 1,5-dibromo-pentane 

Downstream Products

• 21623-88-1 1,1-bis-bromomethyl-cyclohexane 
• 17202-86-7 spiro[2.5]octane-1-carboxylic acid 
• 185-11-5 2-thiaspiro[3.5]nonane 
• 4355-34-4 Cyclohexan-1.1-diacetonitril 

Relevant academic research and scientific papers

Diverse ring opening of thietanes and other cyclic sulfides: An electrophilic aryne activation approach

Organosulfides are a common class of structure units in bioactive molecules and functional materials motivating continuous developments of efficient synthetic methods. Herein, we report an electrophilic aryne-activated ring opening protocol of one or two

Disulfonic acid ester compound for preparing olefin polymerization catalyst

The invention relates to a disulfonic acid ester compound for preparing an olefin polymerization catalyst. The disulfonic acid ester compound is shown in the general formula (I), wherein A and B are carbon or hetero atoms selected from nitrogen, oxygen, s

Laser-Powered Decomposition of Spiroalkanes (n = 2-5)

The laser heating of spiroalkanes (n=2-5) and of their 1,1,2,2-tetradeuterated isotopomers reveals dissimilar modes of their thermal decomposition.Spiropentane decomposes into ethene and propadiene via two competing routes: the direct cleavage and the more important cleavage via intermediary methylenecyclobutane.Spirohexane decomposes through two important concurrent pathways which are the expulsions of ethene from the three-membered ring and a more feasible expulsion of ethene from the four-membered ring.Spiroheptane and spirooctane decompose by a radical-chain mechanism and afford complex mixtures of products; upon addition of propene both compounds rearrange into two cycloalkanes wherein the larger ring of the spiroalkane is preserved and substituted with ethylidene and a vinyl group.