1-Bromo-5-methylhexane
≥95%
- Product Code: 40052
CAS:
35354-37-1
| Molecular Weight: | 179.10 g./mol | Molecular Formula: | C₇H₁₅Br |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00041674 | |
| Melting Point: | Boiling Point: | 168.0±8.0°C at 760 mmHg | |
| Density: | 1.136g/cm3 | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
1-Bromo-5-methylhexane is primarily utilized in organic synthesis as an alkylating agent. It is often employed in the preparation of more complex organic compounds, particularly in the formation of carbon-carbon bonds. The compound is also used in the pharmaceutical industry for the synthesis of intermediates that are further processed into active pharmaceutical ingredients. Additionally, it finds application in the production of specialty chemicals, including surfactants and lubricants, where its alkyl chain can modify the properties of the final product. In research settings, it serves as a reagent in various chemical reactions, including nucleophilic substitution, to study reaction mechanisms and develop new synthetic methodologies.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿4,698.00 |
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| 5.000 | 10-20 days | ฿14,571.00 |
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| 10.000 | 10-20 days | ฿21,879.00 |
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| 25.000 | 10-20 days | ฿39,429.00 |
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1-Bromo-5-methylhexane
1-Bromo-5-methylhexane is primarily utilized in organic synthesis as an alkylating agent. It is often employed in the preparation of more complex organic compounds, particularly in the formation of carbon-carbon bonds. The compound is also used in the pharmaceutical industry for the synthesis of intermediates that are further processed into active pharmaceutical ingredients. Additionally, it finds application in the production of specialty chemicals, including surfactants and lubricants, where its alkyl chain can modify the properties of the final product. In research settings, it serves as a reagent in various chemical reactions, including nucleophilic substitution, to study reaction mechanisms and develop new synthetic methodologies.
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