Dichloroborane methyl sulfide complex

in excess methyl sulfide

Reagent Code: #178335
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CAS Number 63462-42-0

science Other reagents with same CAS 63462-42-0

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Weight 144.86 g/mol
Formula C₂H₇BCl₂S
badge Registry Numbers
MDL Number MFCD00013209
inventory_2 Storage & Handling
Storage Room temperature, argon

description Product Description

Used as a boron-based reagent in organic synthesis, particularly for hydroboration reactions where selective reduction of unsaturated bonds is required. It serves as a source of dichloroborane in a stabilized form, enabling controlled transfer of the BHCl2 group to alkenes and alkynes. This complex is valuable in the preparation of organoboranes that can be further transformed into alcohols, amines, or other functional groups through established downstream reactions. Its stability and reactivity profile make it suitable for use in sensitive transformations where precise boron delivery is needed. Commonly employed in research settings for the development of synthetic methodologies and in the synthesis of complex organic molecules.

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inventory 1g
10-20 days ฿1,540.00

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Dichloroborane methyl sulfide complex
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Used as a boron-based reagent in organic synthesis, particularly for hydroboration reactions where selective reduction of unsaturated bonds is required. It serves as a source of dichloroborane in a stabilized form, enabling controlled transfer of the BHCl2 group to alkenes and alkynes. This complex is valuable in the preparation of organoboranes that can be further transformed into alcohols, amines, or other functional groups through established downstream reactions. Its stability and reactivity profile

Used as a boron-based reagent in organic synthesis, particularly for hydroboration reactions where selective reduction of unsaturated bonds is required. It serves as a source of dichloroborane in a stabilized form, enabling controlled transfer of the BHCl2 group to alkenes and alkynes. This complex is valuable in the preparation of organoboranes that can be further transformed into alcohols, amines, or other functional groups through established downstream reactions. Its stability and reactivity profile make it suitable for use in sensitive transformations where precise boron delivery is needed. Commonly employed in research settings for the development of synthetic methodologies and in the synthesis of complex organic molecules.

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