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Structure of 629626-40-0
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tert-Butyl (2-(2-iodoethoxy)ethyl)carbamate features a reactive iodoethoxy handle flanked by a stable tert-butyl carbamate protecting group, enabling selective conjugation in late-stage functionalization. This bifunctional scaffold integrates seamlessly into peptide and small-molecule synthesis workflows, offering high chemoselectivity under mild conditions.
tert-Butyl (2-(2-iodoethoxy)ethyl)carbamate serves as a versatile bifunctional building block in synthetic chemistry, enabling efficient installation of both protected amine and reactive iodoether handles. The tert-butyl carbamate group provides robust protection for primary amines under standard conditions, while the pendant iodide facilitates palladium-catalyzed coupling reactions such as Suzuki-Miyaura, Stille, or Sonogashira transformations. Its stability during purification and compatibility with diverse reaction environments make it particularly valuable for modular synthesis of complex molecules, including peptide derivatives and functionalized heterocycles.
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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#: 2810
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301-H311-H331-H341
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P361-P405-P501
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Lot numbers can be found on the outside label of a product: