29443-45-6

Usage

General Description

(3,3-dimethylbutan-2-ylidene)hydrazine is a chemical compound with the formula C7H16N2. It is a hydrazine derivative, which means it contains a nitrogen-nitrogen bond. (3,3-dimethylbutan-2-ylidene)hydrazine is used in organic synthesis as a reagent for the preparation of various organic compounds. It is also used as a building block in the production of pharmaceuticals and agrochemicals. Additionally, it has been studied for its potential applications in materials science, particularly in the development of new materials with specific properties. Overall, (3,3-dimethylbutan-2-ylidene)hydrazine has a range of potential uses in various fields due to its reactivity and versatility in chemical reactions.

Upstream product

• 75-97-8 3,3-dimethyl-butan-2-one 
• 917-92-0 3,3-Dimethylbut-1-yne 
• 69498-77-7 3,3-dimethyl-2-butanone N,N-dimethylhydrazone 

Downstream Products

• 75-83-2 2,2-Dimethylbutane 
• 84044-59-7 C₁₃H₁₉N₃*HI 
• 83342-07-8 2-tert-Butyl-2-methyl-5-phenyl-2,3-dihydro-[1,3,4]thiadiazole 
• 75-97-8 3,3-dimethyl-butan-2-one 
• 52756-50-0 C₈H₁₇N₃S 
• 157458-87-2 tert-butylmehylketone-(2,4,6-tri-tert-butylphenyl-fluoroboryl)-hydrazone 
• 594-84-3 2,2-dichloro-3,3-dimethylbutane 
• 594-77-4 2,2-Dibromo-3,3-dimethylbutane 
• 594-81-0 2,3-dibromo-2,3-dimethylbutane 

Relevant academic research and scientific papers

Anti-Bredt N-heterocyclic carbene: An efficient ligand for the gold(i)-catalyzed hydroamination of terminal alkynes with parent hydrazine

An anti-Bredt N-heterocyclic carbene gold(i) chloride complex was synthesized by taking advantage of the reversible insertion of the free carbene into the NH bond of hexamethyldisilazane. This precatalyst promotes the parent hydrazine hydroamination of te

Advantageous Syntheses of Diazo Compounds by Oxidation of Hydrazones with Lead Tetraacetate in Basic Environments

Varied sensitive diazo compounds 3 are produced efficiently and safely in 3-6 g quantities by oxidation (eq 1) of hydrazones 1 at -78 deg C with lead tetraacetate (2) in triethylamine/chloroform, N-methylmorpholine/dimethylformamide, tetramethylguanidine (8)/dimethylformamide, and tetramethylguanidine/methylene chloride, respectively, upon use of appropriate workup and handling techniques.New and improved nonhazardous procedures have been developed for preparing and handling hydrazones 1 from aldehydes and ketones in reactions with excess hydrazine.