1528-34-3

Usage

Uses

Used in Organic Synthesis:
2'-(1-oxopropyl)propionohydrazide is used as a building block for the synthesis of other chemicals and materials, contributing to the development of new compounds with diverse applications.
Used in Pharmaceutical Industry:
2'-(1-oxopropyl)propionohydrazide is used as a precursor for the development of pharmaceuticals, playing a crucial role in the synthesis of new drugs with potential therapeutic benefits.
Used in Agrochemical Industry:
In the agrochemical sector, 2'-(1-oxopropyl)propionohydrazide is utilized as a precursor for the synthesis of agrochemicals, aiding in the creation of effective products for agricultural applications.
Used in Natural Products Synthesis:
2'-(1-oxopropyl)propionohydrazide is employed as a precursor in the synthesis of natural products, facilitating the production of bioactive compounds derived from natural sources.
Used as a Reagent in Chemical Reactions:
2'-(1-oxopropyl)propionohydrazide serves as a reagent in chemical reactions, enabling the formation of new carbon-carbon and carbon-nitrogen bonds, which are essential for the development of novel organic compounds.
Overall, 2'-(1-oxopropyl)propionohydrazide is a multifaceted compound with a wide range of potential uses in the field of organic chemistry, spanning across various industries such as pharmaceuticals, agrochemicals, and natural products synthesis.

Upstream product

• 67-56-1 methanol 
• 118728-47-5 dipropionyl-diazene 
• 5818-15-5 d'hydrazide de l'acide propionique 
• 105-37-3 Ethyl propionate 
• 123-62-6 propionic acid anhydride 
• 802294-64-0 propionic acid 
• 79-03-8 propionyl chloride 

Downstream Products

• 6285-28-5 4-amino-3,5-diethyl-1,2,4-triazole 
• 1615-83-4 1,2-di-n-propylhydrazine 
• 19595-42-7 2,5-diethyl-1,3,4-oxadiazole 
• 73314-40-6 2-ethyl-5-phenyl-1,3,4-oxadiazole 
• 51718-91-3 5-ethyl-1-(3-nitro-phenyl)-1H-tetrazole 
• 4437-51-8 3,4-hexanedione 

Relevant academic research and scientific papers

Conversion of hydrazides into: N, N ′-diacylhydrazines in the presence of a ruthenium(II)-arene complex

Mono and dinuclear p-cymene-ruthenium(ii) complexes [RuCl(L1)(η6-p-cymene)]Cl, where L1 is propionic acid hydrazide (1) and [Ru2Cl2(L2)(η6-p-cymene)2], where H2L2 is N1,N2-dipropionylhydrazine (2), were prepared by a reaction of [RuCl2(η6-p-cymene)]2 with the corresponding ligand precursor. Upon the reaction of [RuCl2(η6-p-cymene)]2 with butyric acid hydrazide and pentanoic acid hydrazide in a 1:1 molar ratio in situ formation of tetradentate bridging ligands, N1,N2-dibutanoylhydrazine and N1,N2-dipentanoylhydrazine, respectively, occurred and the dinuclear complexes [Ru2Cl2(L3)(η6-p-cymene)2] (3) and [Ru2Cl2(L4)(η6-p-cymene)2] (4) were isolated. The compounds were characterised by elemental analysis, ESI-mass spectrometry, IR and 1D and 2D NMR spectroscopies. The structures of all complexes were established using single crystal X-ray crystallography. According to these data in both the mono- and dinuclear complexes the ruthenium atoms adopt the usual three-leg piano-stool geometry which is common for this type of complexes. Combining DFT calculations with the characterisation of the final products using X-ray diffraction, a possible reaction mechanism was discussed.

Parameters of synthesis of hydrazides and 1,2-diacylhydrazines by thermal decomposition of hydrazine salts of aliphatic carboxylic acids

The reaction parameters were refined for synthesis of hydrazides and 1,2-diacylhydrazines by thermal decomposition of salts of aliphatic carboxylic acids of the general formulas RCOOH · N2H4 · H2O and 2RCOOH-N2H4-H2O (R = C2H5-C8H17). Derivatograms for series of compounds were obtained. The effect of hydrazine hydrate excess, temperature, reaction duration, and crystallization conditions on the yield and quality of hydrazides of C7-C9 carboxylic acids was studied.