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Structure of 1375066-73-1
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3-Methyl-1,2,4-thiadiazole-5-carbohydrazide delivers a reactive hydrazide handle paired with a heterocyclic thiadiazole scaffold, enabling efficient conjugation in bioconjugation and coordination chemistry. The methyl substituent enhances solubility and modulates electronic properties, while the bench-stable structure supports reliable performance under standard conditions.
3-Methyl-1,2,4-thiadiazole-5-carbohydrazide serves as a versatile heterocyclic building block for the synthesis of pharmaceutical intermediates and agrochemicals. Its carbohydrazide functionality enables efficient condensation reactions with aldehydes, ketones, and isothiocyanates, facilitating access to diverse thiosemicarbazone derivatives. The molecule exhibits good bench stability and ease of purification, making it suitable for scalable synthesis and high-throughput screening applications.
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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-H312-H315-H319-H332-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P362-P405-P501
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Lot numbers can be found on the outside label of a product: