Product Information
Benzo[b]thiophen-5-ol is a chiral molecule that has been synthesized to be homochiral. It has an active site and selective epoxide hydration activity, which is the rate-limiting step of epoxide ring opening reactions. The mechanism of this reaction is the cleavage of a C-C bond in an epoxide substrate by an O-H or S-H bond in benzo[b]thiophen-5-ol. The nature of this mechanistic bond cleavage reaction is unknown, but it may be due to catalysis by a benzyl group.
Chemical properties
Technical inquiry about: 3D-UAA30135 Benzo[b]thiophen-5-ol
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