22308-11-8

Basic information

• Product Name: cyclohexane-1,1-diylbis(methylene)bis(4-methylbenzenesulfonate)
• Synonyms: cyclohexane-1,1-diylbis(methylene)bis(4-methylbenzenesulfonate)
• CAS NO: 22308-11-8
• Molecular Weight: 452.593
• Mol File: 22308-11-8.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: cyclohexane-1,1-diylbis(methylene)bis(4-methylbenzenesulfonate)(CAS DataBase Reference)
• NIST Chemistry Reference: cyclohexane-1,1-diylbis(methylene)bis(4-methylbenzenesulfonate)(22308-11-8)
• EPA Substance Registry System: cyclohexane-1,1-diylbis(methylene)bis(4-methylbenzenesulfonate)(22308-11-8)

Safety Data

• Hazardous Substances Data: 22308-11-8(Hazardous Substances Data)

Upstream product

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

Downstream Products

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

Relevant articles and documents

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

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.