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Vinylation By 3,6-Dimetyloctin-4-Diol-3,6 Acetylene, Yusupova Lola, Abdukarimova Saida, Rajabov Rustambek, Khalimova Oygul
Vinylation By 3,6-Dimetyloctin-4-Diol-3,6 Acetylene, Yusupova Lola, Abdukarimova Saida, Rajabov Rustambek, Khalimova Oygul
CHEMISTRY AND CHEMICAL ENGINEERING
The aim of the research work elaboration of technology of obtaine of acetylene diols and their vinyl ethers. Reaction of formation mono di vinyl ethers as a result vinyl 3,6-dimetyloktin-4-diol-3,6 by acetylene, and also influence of solvents, the catalyst and its quantity, duration of reaction, temperatures is investigated. Are defined speed of reaction. Recommended vinyl 3,6-dimetyloktin-4-diol-3,6 acetylene in the presence of highly basic systems at atmospheric pressure.
Radiopaque Activity Of Iodine Containing Methylene-Bis-Carbamate, Baltabaev Ubaydulla, Djuraev Abdukahhor, Abduvakilov Jahongir, Abdullaeva Matluba
Radiopaque Activity Of Iodine Containing Methylene-Bis-Carbamate, Baltabaev Ubaydulla, Djuraev Abdukahhor, Abduvakilov Jahongir, Abdullaeva Matluba
CHEMISTRY AND CHEMICAL ENGINEERING
Considering that many derivatives of bis carbamates have different biological activity, it was intuitive to produce a targeted synthesis of new derivatives of bis carbamates by the interaction of hexamethylene diisocyanate with 3,5-diode-4-hydroxybenzoic acid and 2,4,6-triiodophenol (1: 2 mol, respectively) in freshly distilled dry pyridine at 95-110 оC for 6 hours, the corresponding derivatives were obtained - methylene bis carbamates. Experimental studies have been conducted to identify the acute toxicity and radiopaque properties of the synthesized new N, -hexamethylene bis (2,6-diode-4-carboxyphenylcarbamate).
Vinylation By 3,6-Dimetyloctin-4-Diol-3,6 Acetylene, Yusupova Lola, Abdukarimova Saida, Rajabov Rustambek, Khalimova Oygul
Vinylation By 3,6-Dimetyloctin-4-Diol-3,6 Acetylene, Yusupova Lola, Abdukarimova Saida, Rajabov Rustambek, Khalimova Oygul
CHEMISTRY AND CHEMICAL ENGINEERING
The aim of the research work elaboration of technology of obtaine of acetylene diols and their vinyl ethers. Reaction of formation mono di vinyl ethers as a result vinyl 3,6-dimetyloktin-4-diol-3,6 by acetylene, and also influence of solvents, the catalyst and its quantity, duration of reaction, temperatures is investigated. Are defined speed of reaction. Recommended vinyl 3,6-dimetyloktin-4-diol-3,6 acetylene in the presence of highly basic systems at atmospheric pressure.
Radiopaque Activity Of Iodine Containing Methylene-Bis-Carbamate, Baltabaev Ubaydulla, Djuraev Abdukahhor, Abduvakilov Jahongir, Abdullaeva Matluba
Radiopaque Activity Of Iodine Containing Methylene-Bis-Carbamate, Baltabaev Ubaydulla, Djuraev Abdukahhor, Abduvakilov Jahongir, Abdullaeva Matluba
CHEMISTRY AND CHEMICAL ENGINEERING
Considering that many derivatives of bis carbamates have different biological activity, it was intuitive to produce a targeted synthesis of new derivatives of bis carbamates by the interaction of hexamethylene diisocyanate with 3,5-diode-4-hydroxybenzoic acid and 2,4,6-triiodophenol (1: 2 mol, respectively) in freshly distilled dry pyridine at 95-110 оC for 6 hours, the corresponding derivatives were obtained - methylene bis carbamates. Experimental studies have been conducted to identify the acute toxicity and radiopaque properties of the synthesized new N, -hexamethylene bis (2,6-diode-4-carboxyphenylcarbamate).