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Structure of 871332-95-5
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This boronic acid features a chlorine-substituted phenyl ring paired with a cyano group, enabling selective coupling in Suzuki-Miyaura reactions. The electron-deficient aryl system enhances reactivity, while the stable boronate moiety facilitates handling under standard conditions.
(4-Chloro-3-cyanophenyl)boronic acid serves as a versatile building block in Suzuki-Miyaura coupling reactions, enabling efficient C–C bond formation under mild conditions. The molecule combines a boronic acid handle with complementary electron-withdrawing groups—chloro and cyano—offering enhanced reactivity and stability for late-stage functionalization. Its bench-stable nature and tolerance to diverse reaction conditions make it ideal for constructing complex aryl scaffolds in medicinal chemistry and materials science applications.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H315-H319-H335
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Precautionary Statements : P260-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313-P337+P313-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: