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Structure of 6876-00-2
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Biliverdin dihydrochloride was found responsible for cytoprotection. It was also found to induce tolerance to cardiac allografts. Biliverdin hydrochloride may regulate the cellular heme degradation process by occupying the heme binding site on heme oxygenase which would prevent access of the substrate to the catalytic site of the enzyme.
1-Bromo-3-phenoxybenzene serves as a versatile aryl halide building block for Suzuki-Miyaura and Stille coupling reactions, enabling efficient construction of biaryl scaffolds. Its phenoxy substituent enhances solubility and provides orthogonal reactivity, while the bromine functionality offers reliable coupling efficiency under standard catalytic conditions. Bench-stable and readily purified by column chromatography, it facilitates scalable synthesis of functionalized aromatics relevant to agrochemical and materials chemistry applications.
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GHS Pictogram :
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GHS No : GHS05,GHS07,GHS09
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Signal Word : Danger
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UN#: 3082
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Class : 9
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Packing Group : Ⅲ
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Hazard Statements : H315-H317-H318-H335-H411
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Precautionary Statements : P261-P264-P271-P272-P273-P280-P302+P352-P304+P340-P362+P364-P391-P405-P501
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Lot numbers can be found on the outside label of a product: