Hept-6-ynoyl chloride
98%
- Product Code: 131855
CAS:
89856-86-0
| Molecular Weight: | 144.6 g./mol | Molecular Formula: | C₇H₉ClO |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD22041858 | |
| Melting Point: | Boiling Point: | 39-40 °C at 0.4 mmHg | |
| Density: | 1.060±0.06 g/cm3(Predicted) | Storage Condition: | -20°C, Sealed, Inert Gas |
Product Description:
Used primarily as a reactive intermediate in organic synthesis, this compound is valuable for introducing the hept-6-ynoyl functional group into more complex molecules. Its alkyne functionality allows participation in click chemistry reactions, particularly copper-catalyzed azide-alkyne cycloadditions (CuAAC), making it useful in pharmaceutical and agrochemical research for building molecular diversity. The acid chloride group readily reacts with amines and alcohols, enabling the formation of amides and esters, which are common structural motifs in bioactive compounds. It is also employed in the synthesis of specialty polymers and functional materials where terminal alkyne handles are needed for further modification or crosslinking. Due to its reactivity, it is typically handled under inert conditions and used in controlled environments for targeted derivatization.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | £186.35 |
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| 0.250 | 10-20 days | £316.72 |
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| 1.000 | 10-20 days | £855.06 |
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Hept-6-ynoyl chloride
Used primarily as a reactive intermediate in organic synthesis, this compound is valuable for introducing the hept-6-ynoyl functional group into more complex molecules. Its alkyne functionality allows participation in click chemistry reactions, particularly copper-catalyzed azide-alkyne cycloadditions (CuAAC), making it useful in pharmaceutical and agrochemical research for building molecular diversity. The acid chloride group readily reacts with amines and alcohols, enabling the formation of amides and esters, which are common structural motifs in bioactive compounds. It is also employed in the synthesis of specialty polymers and functional materials where terminal alkyne handles are needed for further modification or crosslinking. Due to its reactivity, it is typically handled under inert conditions and used in controlled environments for targeted derivatization.
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