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Structure of 17564-64-6
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N-(Chloromethyl)phthalimide was used:in the synthesis of aminomethyl copoly-(styrene-l%-divinylbenzene) resins of high purityin esterification of 12S-hydroxylabda-8(17),13(16),14-trien-19-oic acid, new labdane-type diterpenoidin esterification of 13-ethoxylabda-8(17),11,14-trien-19-oicacid, new labdane-type diterpenoid
2-(Chloromethyl)isoindoline-1,3-dione serves as a versatile bifunctional building block in synthetic organic chemistry. The chloromethyl group enables nucleophilic substitution reactions, while the phthalimide moiety provides a robust protecting group for amines and participates in standard coupling processes. Its bench-stable nature and compatibility with diverse reaction conditions facilitate efficient synthesis of complex heterocyclic architectures and functionalized intermediates.
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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 : H301-H315-H317-H319-H335-H412
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Precautionary Statements : P261-P264-P270-P271-P272-P273-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: