(Trimethylsilyl)diazomethane
2.0 M solution in Hexanes
- Product Code: 88026
Alias:
(Trimethylsilyl)diazomethane
CAS:
18107-18-1
Properties:
This product comes in a dark glass bottle, not a septum bottle
| Molecular Weight: | 114.22 g./mol | Molecular Formula: | C₄H₁₀N₂Si |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00053946 | |
| Melting Point: | Boiling Point: | 96 °C | |
| Density: | 0.773 g/mL at 25 °C | Storage Condition: | 2~8°C |
Product Description:
(Trimethylsilyl)diazomethane is widely used in organic synthesis as a methylating agent, particularly for converting carboxylic acids into their corresponding methyl esters. This reaction is highly efficient and often occurs under mild conditions, making it a valuable tool in the preparation of esters for further chemical transformations. It is also employed in the synthesis of diazo compounds, which are intermediates in various organic reactions, including cyclopropanation and homologation processes. Additionally, it serves as a precursor for generating carbenes, which are useful in C-H insertion reactions and other catalytic processes. Its stability and ease of handling compared to other diazo compounds make it a preferred choice in laboratory settings.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | liquid |
| CONCENTRATION | 2.0 M |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 25.000 | 10-20 days | $170.68 |
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| 100.000 | 10-20 days | $672.77 |
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| 500.000 | 10-20 days | $2,785.35 |
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(Trimethylsilyl)diazomethane
(Trimethylsilyl)diazomethane is widely used in organic synthesis as a methylating agent, particularly for converting carboxylic acids into their corresponding methyl esters. This reaction is highly efficient and often occurs under mild conditions, making it a valuable tool in the preparation of esters for further chemical transformations. It is also employed in the synthesis of diazo compounds, which are intermediates in various organic reactions, including cyclopropanation and homologation processes. Additionally, it serves as a precursor for generating carbenes, which are useful in C-H insertion reactions and other catalytic processes. Its stability and ease of handling compared to other diazo compounds make it a preferred choice in laboratory settings.
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