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Structure of 28140-60-5
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N-(3-(Phenylamino)allylidene)aniline hydrochloride features a conjugated imine system with an electron-rich phenylamino group, enabling efficient π-delocalization and enhanced stability. This bench-stable salt serves as a key intermediate in the synthesis of functionalized heterocycles and advanced organic semiconductors.
N-(3-(Phenylamino)allylidene)aniline hydrochloride serves as a versatile building block in heterocyclic synthesis, enabling efficient access to substituted indoles and related scaffolds via cyclization reactions. The imine functionality facilitates electrophilic substitution and condensation processes under mild conditions, while the hydrochloride salt enhances solubility and stability for bench-scale handling. Its robust functional group tolerance supports integration into multi-step synthetic sequences.
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302
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Precautionary Statements : P264-P270-P330-P501
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Lot numbers can be found on the outside label of a product: