Potassium ((cyclopropylamino)methyl)trifluoroborate

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Reagent Code: #51685
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CAS Number 1402345-98-5

science Other reagents with same CAS 1402345-98-5

blur_circular Chemical Specifications

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Weight 177.02 g/mol
Formula C₄H₈BF₃KN
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MDL Number MFCD18087754
inventory_2 Storage & Handling
Storage 2-8℃

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Used extensively in organic synthesis, this compound serves as a versatile building block for the introduction of cyclopropylamine groups into target molecules. Its stability and reactivity make it particularly useful in cross-coupling reactions, such as Suzuki-Miyaura coupling, enabling the formation of carbon-carbon bonds in complex organic frameworks. Additionally, it finds application in medicinal chemistry for the development of pharmaceuticals, where the cyclopropyl group can enhance the biological activity and metabolic stability of drug candidates. Its trifluoroborate moiety also contributes to its utility in bioconjugation and labeling techniques.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿32,202.00
inventory 100mg
10-20 days ฿7,263.00
inventory 250mg
10-20 days ฿12,114.00

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Potassium ((cyclopropylamino)methyl)trifluoroborate
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Used extensively in organic synthesis, this compound serves as a versatile building block for the introduction of cyclopropylamine groups into target molecules. Its stability and reactivity make it particularly useful in cross-coupling reactions, such as Suzuki-Miyaura coupling, enabling the formation of carbon-carbon bonds in complex organic frameworks. Additionally, it finds application in medicinal chemistry for the development of pharmaceuticals, where the cyclopropyl group can enhance the biological

Used extensively in organic synthesis, this compound serves as a versatile building block for the introduction of cyclopropylamine groups into target molecules. Its stability and reactivity make it particularly useful in cross-coupling reactions, such as Suzuki-Miyaura coupling, enabling the formation of carbon-carbon bonds in complex organic frameworks. Additionally, it finds application in medicinal chemistry for the development of pharmaceuticals, where the cyclopropyl group can enhance the biological activity and metabolic stability of drug candidates. Its trifluoroborate moiety also contributes to its utility in bioconjugation and labeling techniques.

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