推薦產品
化驗
95%
形狀
liquid
折射率
n20/D 1.414 (lit.)
bp
52-53 °C/175 mmHg (lit.)
密度
0.868 g/mL at 25 °C (lit.)
儲存溫度
2-8°C
SMILES 字串
C[Si](C)(C)N=[N+]=[N-]
InChI
1S/C3H9N3Si/c1-7(2,3)6-5-4/h1-3H3
InChI 密鑰
SEDZOYHHAIAQIW-UHFFFAOYSA-N
相關類別
一般說明
應用
- 通过金属有机化学气相沉积方法制备 GaN 纳米线的氮前驱体。
- Li-O2 电池中的电解质添加剂。TMSN3 的加入可形成坚固的固体电解质界面。
- 这是合成四唑、富勒烯叠氮和 α-叠氮肟的有效试剂。
- 是醇和酚的 O-三甲基甲硅烷基化中的甲硅烷基化度试剂。
訊號詞
Danger
危險分類
Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Flam. Liq. 2
儲存類別代碼
3 - Flammable liquids
水污染物質分類（WGK）
WGK 3
閃點（°F）
42.8 °F - closed cup
閃點（°C）
6 °C - closed cup
個人防護裝備
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
分析證明 (COA)
輸入產品批次/批號來搜索 分析證明 (COA)。在產品’s標籤上找到批次和批號，寫有 ‘Lot’或‘Batch’.。
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文章
The chemistry of organoazides is exceedingly rich, since the azide functionality reacts with electrophiles, nucleophiles, and dipolarophiles, with or without the extrusion of dinitrogen. Common place transformation such as Staudinger reductions or ligations, Cu(I)-catalyzed Huisgen cycloadditions (of the “click” reaction family), Curtius or Schmidt rearrangents, nitrene reactions, or imine formation via aza-Wittig reactions all necessitate organoazide precursors or intermediates
The chemistry of organoazides is exceedingly rich, since the azide functionality reacts with electrophiles, nucleophiles, and dipolarophiles, with or without the extrusion of dinitrogen. Common place transformation such as Staudinger reductions or ligations, Cu(I)-catalyzed Huisgen cycloadditions (of the “click” reaction family), Curtius or Schmidt rearrangents, nitrene reactions, or imine formation via aza-Wittig reactions all necessitate organoazide precursors or intermediates
Organic Azides and Azide Sources
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