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2-(Trimethylsilyl)ethyl 3-Nitro-1H-1,2,4-triazole-1-carboxylate

  • русский язык имя
  • английское имя2-(Trimethylsilyl)ethyl 3-Nitro-1H-1,2,4-triazole-1-carboxylate
  • CAS №1001067-09-9
  • CBNumberCB01570298
  • ФормулаC8H14N4O4Si
  • мольный вес258.31
  • номер MDLMFCD11042686
  • файл Mol1001067-09-9.mol
химическое свойство
растворимость Sol organics (CH2Cl2, THF, CH3CN, EtOAc); reacts with amines.
форма powder to crystal
цвет White to Light yellow
InChI InChI=1S/C8H14N4O4Si/c1-17(2,3)5-4-16-8(13)11-6-9-7(10-11)12(14)15/h6H,4-5H2,1-3H3
ИнЧИКей BHTJYIDOVYPNKR-UHFFFAOYSA-N
SMILES N1(C(OCC[Si](C)(C)C)=O)C=NC([N+]([O-])=O)=N1
Справочник по базе данных CAS 1001067-09-9
Заявления об опасности и безопасности
кода HS 2933.99.9701

2-(Trimethylsilyl)ethyl 3-Nitro-1H-1,2,4-triazole-1-carboxylate химические свойства, назначение, производство

Физические свойства

Mp (dec.) 85–86 °C.

Использование

2-(Trimethylsilyl)ethoxycarbonyl (Teoc) group is one of the most useful protecting groups for amines, which can be cleaved by fluoride ion under neutral conditions. However, 2-(trimethylsilyl)ethyl chloroformate(Teoc-Cl), which is generally used for the introduction of the Teoc protecting group in amines, is quite unstable and easy to decompose; therefore, distillation is recommended at regular intervals. On the other hand, Teoc-NT is a highly stable, nonhygroscopic crystalline material and can be stored for long periods without decomposition. Generally, carbamate formation proceeds quickly under neutral conditions, and highly pure carbamates are obtained without tedious column chromatographic purification. Furthermore, the coproduct 3-nitro-1,2,4-triazole (NT) can be recycled. It participates in the reactions of Reactions with Amines and Aminoalcohols, Amine Protection for Nucleosides, Reaction with Alcohols, etc.

2-(Trimethylsilyl)ethyl 3-Nitro-1H-1,2,4-triazole-1-carboxylate запасные части и сырье

2-(Trimethylsilyl)ethyl 3-Nitro-1H-1,2,4-triazole-1-carboxylate поставщик

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2-(Trimethylsilyl)ethyl 3-Nitro-1H-1,2,4-triazole-1-carboxylate Обзор)