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Structure of 56737-75-8
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This bench-stable hydrazine derivative features a sterically hindered aryl group that enhances reactivity control in coupling processes. The para-methyl substitution pattern increases electron density at the hydrazine nitrogen, facilitating selective imine formation and enabling efficient integration into complex heterocyclic scaffolds under mild conditions.
(2,3-Dimethylphenyl)hydrazine hydrochloride serves as a reliable building block for heterocyclic synthesis, particularly in the construction of pyrazoles and other nitrogen-containing scaffolds. Its stability under standard bench conditions and compatibility with diverse coupling reactions enable efficient access to biologically relevant frameworks. The hydrazine functionality facilitates condensation with carbonyl compounds, offering a practical route to substituted heterocycles used in medicinal chemistry and agrochemical research.
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GHS Pictogram :
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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-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-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: