1726-78-9

Usage

Uses

Used in Chemical Analysis:
DDH is utilized as a chemical reagent for the detection and determination of aldehydes and ketones in various organic compounds. Its ability to form hydrazone derivatives with these carbonyl compounds makes it a valuable tool in analytical chemistry for identifying and quantifying specific organic molecules.
Used in Pharmaceutical Research:
DDH's potential as an antibacterial and anti-cancer agent is currently under investigation. Its unique chemical structure and properties suggest that it may have therapeutic applications in the development of new drugs to combat bacterial infections and cancer.
Used in Organic Synthesis:
Due to its strong nucleophilic nature, DDH can be employed in organic synthesis processes where the formation of hydrazone derivatives is required. This makes it a useful intermediate in the synthesis of complex organic molecules and compounds with specific functional groups.

Upstream product

• 112-54-9 Dodecanal 
• 119-26-6 (2,4-dinitro-phenyl)-hydrazine 
• 33472-15-0 (1-hydroxy-dodecyl)-phosphonic acid di-sec-butyl ester 
• 10161-01-0 1,1-diethoxy-dodeca-2c,6c-diene 
• 124-22-1 n-Dodecylamine 
• 17248-32-7 C₂₄H₄₉N 
• 97-00-7 1-chloro-2,4-dinitro-benzene 
• 112-53-8 1-dodecyl alcohol 
• 68388-21-6 12,13-tetracosanediol 
• 10160-98-2 1,5-undecadiyne 
• 10161-00-9 1,1-diethoxy-dodeca-2,6-diyne 
• 628-16-0 hexa-1,5-diyne 
• 1163304-62-8 1,3-dimethyl-2-undecyl-1H-benzimidazol-3-ium iodide 

Relevant academic research and scientific papers

A novel synthetic method for the preparation of aliphatic aldehydes from the corresponding carboxylic acids

A novel synthetic method for the preparation of aliphatic aldehydes from the corresponding carboxylic acids via 1,3-dimethylbenzimidazolium salts is provided. 1,3-Dimethylbenzimidazolium salts were rapidly reduced with sodium/ethanol and then hydrolyzed with hydrochloric acid to obtain aliphatic aldehydes, in which the 1,3-dimethylbenzimidazolium salts can be readily achieved from the corresponding carboxylic acids. The mechanism for the reductive reaction of 1,3-dimethylbenzimidazolium salts with sodium/ethanol was discussed.

AUTORECYCLING OXIDATION OF AMINES TO CARBONYL COMPOUNDS CATALYZED BY 3,4-DISUBSTITUTED 4-DEAZATOXOFLAVIN DERIVATIVES

3,4-Disubstituted 4-deazatoxoflavin derivatives (II) were prepared by the condensation of 6-(1-methylhydrazino)uracils (I) with appropriate α-diketones.The compounds II oxidized long-chain alkylamines such as n-octylamine and n-dodecylamine besides benzylamine and cyclohexylamine to yield the corresponding carbonyl compounds via imines, catalytically with a markedly high turnover number.