155071
Azidotrimethylsilane
95%
Synonym(s):
Trimethylsilyl azide
About This Item
Recommended Products
Assay
95%
form
liquid
refractive index
n20/D 1.414 (lit.)
bp
52-53 °C/175 mmHg (lit.)
density
0.868 g/mL at 25 °C (lit.)
storage temp.
2-8°C
SMILES string
C[Si](C)(C)N=[N+]=[N-]
InChI
1S/C3H9N3Si/c1-7(2,3)6-5-4/h1-3H3
InChI key
SEDZOYHHAIAQIW-UHFFFAOYSA-N
General description
Application
- A nitrogen precursor to prepare GaN nanowire via metal-organic chemical vapor deposition method.
- An electrolyte additive in Li-O2 batteries. The addition of TMSN3 results in the formation of robust solid electrolyte interphase.
- An efficient reagent in the synthesis of tetrazoles, fullerenyl azide, and α-azido oximes.
- A silylating agent in the O-trimethyl silylation of alcohols and phenols.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Flam. Liq. 2
Storage Class Code
3 - Flammable liquids
WGK
WGK 3
Flash Point(F)
42.8 °F - closed cup
Flash Point(C)
6 °C - closed cup
Personal Protective Equipment
Certificates of Analysis (COA)
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Articles
Click chemistry, and the copper(I)-catalyzed azide-alkyne cycloaddition (CuAAC) in particular, is a powerful new synthetic tool in polymer chemistry and material science.
Since the preparation of the first organic azide, phenyl azide, by Peter Griess in 1864 this energy-rich and versatile class of compounds has enjoyed considerable interest.
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