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CAS RN: 87576-94-1 | Product Number: T1184
Trimethylsilylmethyl Azide
Purity: >97.0%(GC)
Synonyms:
- Azidomethyltrimethylsilane
Product Documents:
Size | Unit Price | Belgium | Japan* | Quantity |
---|---|---|---|---|
1G |
€81.00
|
4 | 21 |
|
5G |
€262.00
|
≥40 | ≥40 |
|
*Stock available in Belgium will be delivered in 1 to 3 days
*Stock available in Japan will be delivered in 1 to 2 weeks (excludes regulated items and dry ice shipments).
Product Number | T1184 |
Purity / Analysis Method | >97.0%(GC) |
Molecular Formula / Molecular Weight | C__4H__1__1N__3Si = 129.24 |
Physical State (20 deg.C) | Liquid |
Storage Temperature | Room Temperature (Recommended in a cool and dark place, <15°C) |
Store Under Inert Gas | Store under inert gas |
Condition to Avoid | Moisture Sensitive |
CAS RN | 87576-94-1 |
Reaxys Registry Number | 4229991 |
PubChem Substance ID | 87576967 |
MDL Number | MFCD00059964 |
Specifications
Appearance | Colorless to Yellow to Green clear liquid |
Purity(GC) | min. 97.0 % |
Properties (reference)
Boiling Point | 60 °C/82.5 mmHg |
Flash point | 6 °C |
Specific Gravity (20/20) | 0.87 |
Refractive Index | 1.43 |
GHS
Pictogram | |
Signal Word | Danger |
Hazard Statements | H225 : Highly flammable liquid and vapour. |
Precautionary Statements | P501 : Dispose of contents/ container to an approved waste disposal plant. P210 : Keep away from heat, hot surfaces, sparks, open flames and other ignition sources. No smoking. P233 : Keep container tightly closed. P370 + P378 : In case of fire: Use dry sand, dry chemical or alcohol-resistant foam to extinguish. P303 + P361 + P353 : IF ON SKIN (or hair): Take off immediately all contaminated clothing. Rinse skin with water. P403 + P235 : Store in a well-ventilated place. Keep cool. |
Related Laws:
Transport Information:
UN Number | UN1993 |
Class | 3 |
Packing Group | II |
HS Number | 2931900090 |
Application
Aminating Agent
Experimental procedure4): To a solution of veratrole (30 mL, 234 mmol) and N,N,N',N'-tetramethylethylenediamine (35.4 mL, 234 mmol) in ether (240 mL) is added dropwise over 15 min n-butyllithium (2.47 mol/L hexane solution, 94.8 mL, 234 mmol) at 0 °C under an N2 atmosphere. The resulting suspension is stirred at 22 °C for 18.5 h and then recooled to 0 °C. A solution of trimethylsilylmethyl azide (33.6 mL, 234 mmol) in ether (120 mL) is added dropwise over 10 min into the mixture. The resulting solution is warmed to 22 °C, stirred for an additional 3.5 h, and poured into water (200 mL). The organic layer is extracted with 1 mol/L HCl (5 x 100 mL), and the combined aqueous extracts are made basic to litmus with 3 mol/L NaOH and extracted with ether (5 x 100 mL). The combined ether extracts are washed with water (150 mL), brine (150 mL) and then dried over MgSO4. Evaporation of the solvent followed by Kugelrohr distillation gives 2,3-dimethoxyaniline (28.3 g, 78% yield).
References
- 1)Synthesis and reactions of trimethylsilylmethyl azide
- 2)A SILYL-FUNCTIONALIZED ALKYL AZIDE, TRIMETHYLSILYLMETHYL AZIDE; SYNTHESIS AND CYCLOADDITION REACTION TO ACETYLENIC DIPOLAROPHILES
- 3)One-pot synthesis of N-[(trimethylsilyl)methyl]imines and (trimethylsilyl)methyl-substituted heterocumulenes from (trimethylsilyl)methyl azide
- 4)A synthesis of aaptamine
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