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2,8,9-TRIMETHYL-2,5,8,9-TETRAAZA-1- &
Кат. №: 463558-5G
Производитель: Sigma-Aldrich
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2,8,9-TRIMETHYL-2,5,8,9-TETRAAZA-1- &
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Кат. №: 463558-5G
Производитель: Sigma-Aldrich
Кол-во:
Цена по запросу
Товар оформляется под заказ
Main image
Печать
2,8,9-TRIMETHYL-2,5,8,9-TETRAAZA-1- &
Кат. №: 463558-5G
Производитель: Sigma-Aldrich
Кол-во:
Цена по запросу
Товар оформляется под заказ
Description Application 2,8,9-Trimethyl-2,5,8,9-tetraaza-1-phosphabicyclo[3.3.3]undecane is involved as a reactant in: • Studies of N-heterocyclic carbene ligand effects on metal hydride bond energies. • Synthesis of heterogenous basic catalysts immobilized on SBA-15 silica. • Protection / deprotection strategies for diazeniumdiolate chemistry. • Encaging of the molecule to study the change in its catalytic ability. • C-N coupling reactions. • Derivative synthesis used as a promoter for aza and thia-Michael reaction and Strecker reaction. Reactant involved in: • Studies of N-heterocyclic carbene ligand effects on metal hydride bond energies • Synthesis of heterogenous basic catalysts immobilized on SBA-15 silica • Protection / deprotection strategies for diazeniumdiolate chemistry • Encaging of the molecule to study change in its catalytic ability • C-N coupling reactions • Derivative synthesis used as a promoter for aza and thia-Michael reaction and Strecker reaction Packaging 1, 5 g in glass bottle
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Acids & Bases, Bases, Chemical Synthesis, Organic Bases, Synthetic Reagents More... Quality Level
Дорогой клиент, на сайте внедрена нейросеть для сбора информации о товаре. Это может привести к незначительным расхождениям в характеристиках продукции.
Description Application 2,8,9-Trimethyl-2,5,8,9-tetraaza-1-phosphabicyclo[3.3.3]undecane is involved as a reactant in: • Studies of N-heterocyclic carbene ligand effects on metal hydride bond energies. • Synthesis of heterogenous basic catalysts immobilized on SBA-15 silica. • Protection / deprotection strategies for diazeniumdiolate chemistry. • Encaging of the molecule to study the change in its catalytic ability. • C-N coupling reactions. • Derivative synthesis used as a promoter for aza and thia-Michael reaction and Strecker reaction. Reactant involved in: • Studies of N-heterocyclic carbene ligand effects on metal hydride bond energies • Synthesis of heterogenous basic catalysts immobilized on SBA-15 silica • Protection / deprotection strategies for diazeniumdiolate chemistry • Encaging of the molecule to study change in its catalytic ability • C-N coupling reactions • Derivative synthesis used as a promoter for aza and thia-Michael reaction and Strecker reaction Packaging 1, 5 g in glass bottle
Related Categories
Acids & Bases, Bases, Chemical Synthesis, Organic Bases, Synthetic Reagents More... Quality Level
Дорогой клиент, на сайте внедрена нейросеть для сбора информации о товаре. Это может привести к незначительным расхождениям в характеристиках продукции.