Sodium cyclobutanesulfinate

98%

Reagent Code: #232424
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CAS Number 1352077-20-3

science Other reagents with same CAS 1352077-20-3

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Weight 142.15 g/mol
Formula C₄H₇NaO₂S
inventory_2 Storage & Handling
Storage Room temperature, light-proof, inert gas

description Product Description

Used as a key reagent in organic synthesis, particularly in radical reactions. It serves as a source of cyclobutyl radicals when combined with transition metal catalysts or under photoredox conditions. This enables the cyclobutylation of aryl, heteroaryl, and alkenyl halides, which is valuable in medicinal chemistry for building strained ring systems. Its stability and ease of handling make it suitable for scalable transformations in drug discovery and development. Also employed in decarboxylative and dehalogenative couplings to introduce cyclobutane motifs into complex molecules, enhancing structural diversity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,250.00
inventory 1g
10-20 days ฿30,990.00
inventory 5g
10-20 days ฿108,780.00

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Sodium cyclobutanesulfinate
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Used as a key reagent in organic synthesis, particularly in radical reactions. It serves as a source of cyclobutyl radicals when combined with transition metal catalysts or under photoredox conditions. This enables the cyclobutylation of aryl, heteroaryl, and alkenyl halides, which is valuable in medicinal chemistry for building strained ring systems. Its stability and ease of handling make it suitable for scalable transformations in drug discovery and development. Also employed in decarboxylative and dehal
Used as a key reagent in organic synthesis, particularly in radical reactions. It serves as a source of cyclobutyl radicals when combined with transition metal catalysts or under photoredox conditions. This enables the cyclobutylation of aryl, heteroaryl, and alkenyl halides, which is valuable in medicinal chemistry for building strained ring systems. Its stability and ease of handling make it suitable for scalable transformations in drug discovery and development. Also employed in decarboxylative and dehalogenative couplings to introduce cyclobutane motifs into complex molecules, enhancing structural diversity.
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