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Structure of 14871-41-1
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BP Fluor 350 Picolyl Azide is a blue-fluorescent azide-activated probe that reacts with terminal alkynes via a copper-catalyzed click reaction (CuAAC). It also reacts with strained cyclooctyne via a copper-free click chemistry reaction to form a stable triazole and does not require Cu-catalyst or elevated temperatures.
Carbonylchlorobis(triphenylphosphine)iridium(I) serves as a well-established precatalyst in homogeneous iridium-catalyzed transformations, particularly in hydrogenation and C–H functionalization reactions. Its bench-stable nature, tolerance to air and moisture under controlled conditions, and predictable reactivity facilitate reliable catalytic turnover. The ligand environment enables selective activation of H₂ and polar substrates, making it a practical choice for synthetic workflows requiring robust and reproducible catalysis.
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GHS Pictogram :
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GHS No : GHS06
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H302-H312-H331
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P363-P405-P501
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Lot numbers can be found on the outside label of a product: