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Structure of 41103-17-7
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4-Chloropyrimidine-5-carboxylic acid ethyl ester features a chlorinated pyrimidine core paired with an ester-functionalized carboxylic acid, enabling direct incorporation into heterocyclic synthesis. The electron-deficient pyrimidine ring facilitates nucleophilic substitution reactions, while the ethyl ester group serves as a handle for subsequent derivatization. This compound exhibits excellent stability under standard bench conditions and is compatible with common reaction protocols in medicinal chemistry and materials science.
4-Chloropyrimidine-5-carboxylic acid ethyl ester serves as a versatile building block in heterocyclic synthesis, enabling efficient access to pyrimidine-based scaffolds. Its chloro and ester functionalities support sequential functionalization via nucleophilic substitution and hydrolysis, facilitating the construction of pharmaceutically relevant intermediates. The compound exhibits good bench stability and is compatible with standard reaction conditions, simplifying purification and integration into multi-step synthetic sequences.
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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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: