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Structure of 765-09-3
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1-Bromotridecane was used in the synthesis of:tetradecanoic acid enriched with 13C at carbons 1, 3, or 6(Z)-7-henicosene(Z)-(2R)-[N-carboethoxypyrrolidine]tetradec-1-ene2,3,6,7,10,11,14,15-octaalkyloxytetrabenzo[a,d,g,jlcyclododecatetraenes (CTTV-n) containing n=4-15 methylenic units in the alkyloxy substituents
1-Bromotridecane serves as a versatile C13 alkylating agent, enabling efficient introduction of long-chain alkyl groups in synthetic transformations. Its primary utility lies in nucleophilic substitution reactions, where it functions reliably with amines, thiols, and carbanions under standard conditions. The compound exhibits good bench stability and facilitates straightforward purification, making it well-suited for applications in surfactant synthesis, lipid chemistry, and the construction of complex organic architectures requiring extended hydrocarbon linkages.
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GHS Pictogram :
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GHS No : GHS05,GHS07
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Signal Word : Danger
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UN#: 1760
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H302-H315-H318-H335
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Precautionary Statements : P260-P264-P270-P271-P280-P301+P310-P302+P352-P304+P340-P305+P351+P338-P310-P312-P330-P332+P313-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: