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Structure of 927670-97-1
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The reaction of phenylmercury (II) chloride with acetophenonethiosemicarbazone (Hatsc) in ethanol in 1: 1 mole ratio undergoes symmetrisation forming the products, HgCl2 (Hatse) 2 and Ph2Hg instead of the anticipated compound PhHgCl (Hatse). A new method for the determination of chloride ion is based on the formation of phenylmercury(II) chloride, its extraction into chloroform and reaction with sodium diethyldithiocarbamate to form phenylmercury(II) diethyldithiocarbamate.
Thalidomide-NH-CH₂-COOH serves as a versatile scaffold for targeted molecular diversification, enabling the construction of imide-based heterocycles and peptide conjugates. Its amide and carboxylic acid functionalities facilitate robust coupling reactions, offering enhanced solubility and metabolic stability in medicinal chemistry applications.
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GHS Pictogram :
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GHS No : GHS06,GHS08
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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 : H301-H312-H361
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Precautionary Statements : P264-P270-P280-P302+P352-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: