27905-76-6

Upstream product

• 51594-55-9 (R)-(-)-epichlorohydrin 
• 107-07-3 2-chloro-ethanol 
• 7664-93-9 sulfuric acid 
• 106-89-8 epichlorohydrin 

Downstream Products

• 5412-14-6 3-(β-Chloroethoxy)-1,2-epoxypropane 
• 406913-93-7 [(2S)-1,4-dioxan-2-yl]methanol 
• 93405-71-1 Phosphorigsaeure-<2-(2-chlor-aethoxy)-1-chlormethyl-aethylester>-diphenylester 
• 250340-68-2 1-(2-chloroethoxy)-2-tosyl-3-azidopropane 
• 250340-69-3 1-(2-chloroethoxy)-2-tosyl-3-methoxypropane 
• 21048-16-8 2-(chloromethyl)-1,4-dioxane 
• 29908-11-0 (+/-)-2-(hydroxymethyl)-1,4-dioxane 

Relevant academic research and scientific papers

Synthesis of N-3-chloroalkoxy-2-nitroxypropyl-N-alkylnitramines and their subsequent azidation

Nitration of N-3-chloroalkoxy-2-hydroxypropyl-N-alkylsulfamates gave the corresponding N-3-chloroalkoxy-2-nitroxypropyl-N-alkylnitramines. Azidation of the latter resulted in N-azido-3-azidoalkoxypropyl-N-alkylnitramines.

Absorbent solution based on beta-hydroxylated tertiary diamines and method of removing acid compounds from a gaseous effluent

An absorbent solution is provided for removing acid compounds contained in a gaseous effluent and a method of removing acid compounds contained in a gaseous effluent contacts the gaseous effluent with the absorbent solution. The absorbent solution includes at least one of the following two nitrogen compounds belonging to the family of tertiary diamines: 1-dimethylamino-3-(2-dimethylaminoethoxy)-2-propanol 1,1′-oxybis[3-(dimethylamino)-2-propanol] and water.

Heterocylic antiviral compounds

This invention relates to piperidine derivatives of formula I wherein R1, R2, R3 and R4 are as defined herein useful in the treatment of a variety of disorders, including those in which the modulation of CCR5 re

Synthesis of Substituted Dithia-9-crown-3-ethers

Diethylene glycol monochlorides were prepared from epoxides by action of the chloroethanol. Their conversion into substituted dithia-9-crown-3-ethers has been realized by treatment with p-toluenesulfonyl chloride, followed by the action of 1,2-dimercaptoe

SYNTHESIS OF OLIGO(ETHYLENE GLYCOL) DERIVATIVES

Oligo(ethylene glycol) derivatives were obtained by the reaction of oligo(ethylene glycol) chlorohydrins with epichlorohydrin using H2SO4 catalyst and sunsequent treatment with NaOH in ether solution.The structure of the obtained products was characterized by 13C NMR and IR spectra.

RADICAL THIYLATION OF SOME UNSATURATED 1,3-DIOXOLANES

The radical addition of thiols to unsaturated 1,3-dioxolanes leads to the formation of the products from addition against the Markovnikov rule.Identical thioethers are produced as a result of nucleophilic substitution of the corresponding chloromethyl derivatives of 1,3-dioxolanes by sodium butanethiolate or phenylmethanethiolate.

REACTIONS OF 1-CHLORO-2,3-EPOXYPROPANE WITH ALCOHOLS IN THE PRESENCE OF STANNIC CHLORIDE. II. DISTRIBUTION OF THE ADDITION PRODUCTS AND THE RELATIVE ACTIVITY OF THE ALCOHOLS

In the distribution of the products from the reaction of 1-chloro-2,3-epoxypropane with alcohols in the presence of stannic chloride the determining factor is their capacity for complex formation with stannic chloride.This is confirmed by a correlation between the independently determined relative reaction constants and the constants for exchange of the alcohols and the complexes with stannic chloride.

MACROHETEROCYCLES. SYNTHESIS OF MACROCYCLES CONTAINIG HYDROXYL GROUPS IN THE POLYETHER RING

Four new macrocyclic polyethers containing hydroxyl groups in the polyether ring were obtained by the reaction of pyrocatechol and bis(2-o-hydroxyphenoxyethyl)ether with 1,6-dichloro-4-oxa-2-hexanol and 1,10-dichloro-4,7-dioxa-2,9-decanediol.Features of their extraction capacity in relation to alkali and alkaline-earth metals were investigated.