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Structure of 870-24-6
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Glycolaldehyde dimer may be used in the synthesis of 3,4-diaza-2-hexene-1,6-diol, which can undergo hydrogenation to form 1,2-bis(2-hydroxyethyl)hydrazine. It undergoes cycloaddition with 2,3-dihydrofuran in the presence of a chiral catalyst to form fused bicyclic tetrahydrofuran (bis-THF) alcohol, a key moiety of HIV protease inhibitors.
2-Chloroethanamine hydrochloride serves as a versatile bifunctional building block in synthetic organic chemistry, enabling efficient construction of nitrogen-containing heterocycles and peptide analogs. Its reactive chloroethyl group facilitates alkylation reactions under mild conditions, while the amine functionality offers facile derivatization. The hydrochloride salt form ensures excellent bench stability, ease of handling, and compatibility with standard aqueous workups, making it well-suited for use in medicinal chemistry and process development workflows.
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GHS Pictogram :
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GHS No : GHS05,GHS08
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Signal Word : Danger
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UN#: 3261
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H290-H314-H341
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Precautionary Statements : P234-P260-P264-P280-P301+P330+P331-P304+P340-P363-P390-P405-P406-P501
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Lot numbers can be found on the outside label of a product: