Bromotriphenylmethane
98%
- Product Code: 78316
Alias:
Triphenyl bromide; trityl bromide
CAS:
596-43-0
| Molecular Weight: | 323.23 g./mol | Molecular Formula: | C₆H₅₃CBr |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00000120 | |
| Melting Point: | 152-154 °C | Boiling Point: | 230 °C/15 mmHg |
| Density: | 1.55 g/cm3 | Storage Condition: | 2~8°C |
Product Description:
Bromotriphenylmethane is primarily used in organic synthesis as a reagent for the generation of triphenylmethyl (trityl) cations. These cations are highly stable and serve as effective protecting groups for alcohols in complex multi-step organic reactions. The compound is also utilized in the study of reaction mechanisms, particularly in carbocation chemistry, due to the stability of the trityl cation. Additionally, it finds application in the preparation of specialized polymers and as a starting material for the synthesis of various trityl derivatives used in pharmaceuticals and materials science. Its role in facilitating selective reactions and protecting functional groups makes it a valuable tool in synthetic organic chemistry.
Product Specification:
| Test | Specification |
|---|---|
| Purity | 97.5-100 |
| Appearance | White to yellow powder |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿300.00 |
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| 5.000 | 10-20 days | ฿720.00 |
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| 25.000 | 10-20 days | ฿2,540.00 |
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| 100.000 | 10-20 days | ฿10,060.00 |
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| 500.000 | 10-20 days | ฿31,920.00 |
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Bromotriphenylmethane
Bromotriphenylmethane is primarily used in organic synthesis as a reagent for the generation of triphenylmethyl (trityl) cations. These cations are highly stable and serve as effective protecting groups for alcohols in complex multi-step organic reactions. The compound is also utilized in the study of reaction mechanisms, particularly in carbocation chemistry, due to the stability of the trityl cation. Additionally, it finds application in the preparation of specialized polymers and as a starting material for the synthesis of various trityl derivatives used in pharmaceuticals and materials science. Its role in facilitating selective reactions and protecting functional groups makes it a valuable tool in synthetic organic chemistry.
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