rel-((1R,2S)-2-Methylcyclopropyl)boronicacid

98%

Reagent Code: #232011
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CAS Number 1309366-01-5

science Other reagents with same CAS 1309366-01-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 99.92 g/mol
Formula C₄H₉BO₂
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used in Suzuki-Miyaura cross-coupling reactions to introduce the (1R,2S)-2-methylcyclopropyl group into organic molecules, enabling the synthesis of chiral cyclopropane-containing compounds. These structures are valuable in pharmaceutical development due to their metabolic stability and conformational rigidity. The boronic acid serves as a key building block for creating bioactive molecules, particularly in the design of drugs targeting central nervous system disorders and antiviral agents. Its stereospecific structure allows for precise control over molecular geometry in synthetic pathways.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿14,300.00
inventory 250mg
10-20 days ฿23,720.00
inventory 1g
10-20 days ฿59,820.00
rel-((1R,2S)-2-Methylcyclopropyl)boronicacid
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Used in Suzuki-Miyaura cross-coupling reactions to introduce the (1R,2S)-2-methylcyclopropyl group into organic molecules, enabling the synthesis of chiral cyclopropane-containing compounds. These structures are valuable in pharmaceutical development due to their metabolic stability and conformational rigidity. The boronic acid serves as a key building block for creating bioactive molecules, particularly in the design of drugs targeting central nervous system disorders and antiviral agents. Its stereospe

Used in Suzuki-Miyaura cross-coupling reactions to introduce the (1R,2S)-2-methylcyclopropyl group into organic molecules, enabling the synthesis of chiral cyclopropane-containing compounds. These structures are valuable in pharmaceutical development due to their metabolic stability and conformational rigidity. The boronic acid serves as a key building block for creating bioactive molecules, particularly in the design of drugs targeting central nervous system disorders and antiviral agents. Its stereospecific structure allows for precise control over molecular geometry in synthetic pathways.

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