159239-28-8

Basic information

• Product Name: 2-Furancarboxylicacid,2,2-dimethylhydrazide(9CI)
• Synonyms: 2-Furancarboxylicacid,2,2-dimethylhydrazide(9CI)
• CAS NO: 159239-28-8
• Molecular Formula: C7H10N2O2
• Molecular Weight: 154.17
• Product Categories: AMIDE
• Mol File: 159239-28-8.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-Furancarboxylicacid,2,2-dimethylhydrazide(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Furancarboxylicacid,2,2-dimethylhydrazide(9CI)(159239-28-8)
• EPA Substance Registry System: 2-Furancarboxylicacid,2,2-dimethylhydrazide(9CI)(159239-28-8)

Safety Data

• Hazardous Substances Data: 159239-28-8(Hazardous Substances Data)

Usage

General Description

2-Furancarboxylic acid, 2,2-dimethylhydrazide (9CI) is a chemical compound with the molecular formula C7H10N2O3. It is a derivative of furan and is commonly known as dimethyloxalyl hydrazide (DMOH). 2-Furancarboxylicacid,2,2-dimethylhydrazide(9CI) is used as a herbicide, specifically as a growth regulator for rice crops to prevent the growth of undesired grasses. It works by inhibiting the biosynthesis of gibberellins, a plant hormone responsible for cell elongation and division. DMOH is also utilized in the process of synthesizing other organic compounds. Additionally, it has potential applications in the pharmaceutical industry due to its ability to inhibit the growth of tumor cells. However, it is important to note that this compound should be handled and used with caution, as it may have harmful effects on human health and the environment.

Upstream product

• 527-69-5 2-furancarbonyl chloride 
• 57-14-7 N,N-Dimethylhydrazine 

Relevant articles and documents

N-Ammonium Ylide Mediators for Electrochemical C-H Oxidation

The site-specific oxidation of strong C(sp3)-H bonds is of uncontested utility in organic synthesis. From simplifying access to metabolites and late-stage diversification of lead compounds to truncating retrosynthetic plans, there is a growing need for new reagents and methods for achieving such a transformation in both academic and industrial circles. One main drawback of current chemical reagents is the lack of diversity with regard to structure and reactivity that prevents a combinatorial approach for rapid screening to be employed. In that regard, directed evolution still holds the greatest promise for achieving complex C-H oxidations in a variety of complex settings. Herein we present a rationally designed platform that provides a step toward this challenge using N-ammonium ylides as electrochemically driven oxidants for site-specific, chemoselective C(sp3)-H oxidation. By taking a first-principles approach guided by computation, these new mediators were identified and rapidly expanded into a library using ubiquitous building blocks and trivial synthesis techniques. The ylide-based approach to C-H oxidation exhibits tunable selectivity that is often exclusive to this class of oxidants and can be applied to real-world problems in the agricultural and pharmaceutical sectors.

Uphill Transport of Metal Picrate through a Liquid Membrane by Ylides

New pH dependent carrier nolecules, aminimides, were synthesized, and their properties were investigated by transport experiments of metal picrate through a liquid membrane.These aminimides have the nitrogen atom bearing a negative charge (ylidic nitrogen