1113-63-9

Usage

Uses

Used in Pharmaceutical Industry:
2-METHYLMALONAMIDE is used as a key intermediate in the synthesis of pharmaceuticals for its ability to facilitate the creation of diverse medicinal compounds. Its role in drug development is crucial, as it can be incorporated into the molecular structures of various therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical sector, 2-METHYLMALONAMIDE is utilized as an intermediate in the production of pesticides and other agricultural chemicals, contributing to the development of effective solutions for crop protection and enhancement of agricultural yields.
Used in Water Treatment:
2-METHYLMALONAMIDE is used as a corrosion inhibitor in water treatment processes to protect metal surfaces from degradation, thereby extending the lifespan of water infrastructure and ensuring the efficiency of water delivery systems.
Used in Adhesive Production:
In the manufacturing of industrial adhesives, 2-METHYLMALONAMIDE is employed to enhance the adhesive's properties, such as bonding strength and durability, making it suitable for a wide range of applications in various industries.

InChI:InChI=1/C4H8N2O2/c1-2(3(5)7)4(6)8/h2H,1H3,(H2,5,7)(H2,6,8)

Upstream product

• 609-02-9 methyl-malonic acid dimethylester 
• 609-08-5 Diethyl methylmalonate 
• 67-56-1 methanol 
• 108-13-4 malonodiamide 
• 124-41-4 sodium methylate 
• 74-88-4 methyl iodide 
• 2417-22-3 5-methylbarbituric acid 
• 7664-41-7 ammonia 
• 516-05-2 methyl-propanedioic acid 

Downstream Products

• 3696-36-4 2-methylmalononitrile 
• 18337-63-8 4-hydroxy-5-methylpyrimidin-6(1H)-one 
• 2400-78-4 1,3-diamino-2-methylpropane 

Relevant academic research and scientific papers

Corresponding amine nitrile and method of manufacturing thereof

The invention relates to a preparation method of nitrile. Compared with the prior art, the preparation method has the characteristics of obvious reduction of the usage amount of ammonia sources, low environmental pressure, low energy consumption, low production cost, high purity and yields of nitrile products, and the like, and can be used for obtaining nitrile with a more complex structure. The invention also relates to a method for preparing corresponding amine with nitrile.

Corresponding amine nitrile and method of manufacturing thereof (by machine translation)

The present invention relates to a nitrile manufacturing method, which has characteristics of significantly-reduced ammonia source consumption, low environmental pressure, low energy consumption, low production cost, high nitrile purity, high nitrile yield and the like compared with the method in the prior art, wherein nitrile having a complicated structure can be obtained through the method. The present invention further relates to a method for producing a corresponding amine from the nitrile.

Corresponding amine nitrile and method of manufacturing thereof

The invention relates to a preparation method of nitrile. Compared with the prior art, the preparation method has the characteristics of obvious reduction of the usage amount of ammonia sources, low environmental pressure, low energy consumption, low production cost, high purity and yields of nitrile products, and the like, and can be used for obtaining nitrile with a more complex structure. The invention also relates to a method for preparing corresponding amine with nitrile.

Tetrapodal amidoxime ligands I. Coordination isomerism due to self-complementary dimerization of a pyramidal cobalt(iii) coordination module

A bis-μ-amidoximato-bridged cobalt(iii) dimer obtained with a new tetrapodal ligand possesses interesting structural parameters as a consequence of intramolecular hydrogen bonding intentionally built into the complex. Its synthesis and properties are described. The new ligand type combines attributes of two previously described ligand classes: It binds a metal ion in a tetrapodal pentadentate fashion and forms a pseudomacrocycle through hydrogen bonds, characteristic of chelating oxime ligands. Coordination isomerism, which is a consequence of dimer formation, has been analyzed by means of X-ray crystallography and carbon-13 nuclear magnetic resonance spectroscopy. The Royal Society of Chemistry 2012.

Processes for preparing aromatic ethers

The present invention relates to processes for preparing aromatic ether compounds that are modulators of glucose metabolism and therefore useful in the treatment of metabolic disorders such as diabetes and obesity.

Diagnostic imaging methods using rhenium and technetium complexes containing a hypoxia-localizing moiety

Novel methods, processes and metal complexes attached to a hypoxia-localizing moiety comprising a metal, preferably radionuclide of rhenium or technetium; a hypoxia-localizing moiety; and, a complexing ligand, wherein said ligand and said radionuclide combined have cell membrane permeabilities greater than that of sucrose, are disclosed.

Chemistry of alpha-aminonitriles. Aziridine-2-carbonitrile: photochemical formation from 2-aminopropenenitrile

2-Aminopropenenitrile in solvents such as MeCN, MeOH, or H2O is photoisomerized by UV light to racemic aziridine-2-carbonitrile (rac-2); the larger part of the starting material, however, fragments to HCN and MeCN. The observed photocyclization constitutes a structural connection within an ensemble of C3H4N2 compounds considered to be potentially relevant to prebiotic chemistry.