2,2,3,3-Tetramethylcyclopropanecarbonyl chloride
≥95%
- Product Code: 238631
CAS:
24303-61-5
Molecular Weight: | 160.6412 g./mol | Molecular Formula: | C₈H₁₃ClO |
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EC Number: | MDL Number: | MFCD00012257 | |
Melting Point: | Boiling Point: | 153 °C | |
Density: | 1.028 g/cm3 | Storage Condition: | 2-8°C, Inert Gas |
Product Description:
Used primarily as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, this acyl chloride derivative enables the introduction of sterically hindered cyclopropane moieties into larger molecules. Its high ring strain and dense alkyl substitution make it valuable for constructing bioactive compounds where metabolic stability and conformational rigidity are desired. It is often employed in Friedel-Crafts acylation and nucleophilic substitution reactions to form ketones or amides in complex molecule assembly. Due to its reactivity, it is handled under anhydrous conditions and used in controlled environments for targeted derivatization in research and development settings.
Sizes / Availability / Pricing:
Size | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿1,480.00 |
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0.250 | 10-20 days | ฿2,360.00 |
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1.000 | 10-20 days | ฿8,280.00 |
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5.000 | 10-20 days | ฿37,260.00 |
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25.000 | 10-20 days | ฿149,040.00 |
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2,2,3,3-Tetramethylcyclopropanecarbonyl chloride
Used primarily as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, this acyl chloride derivative enables the introduction of sterically hindered cyclopropane moieties into larger molecules. Its high ring strain and dense alkyl substitution make it valuable for constructing bioactive compounds where metabolic stability and conformational rigidity are desired. It is often employed in Friedel-Crafts acylation and nucleophilic substitution reactions to form ketones or amides in complex molecule assembly. Due to its reactivity, it is handled under anhydrous conditions and used in controlled environments for targeted derivatization in research and development settings.
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