cas 52798-47-7|| where to buy methyl 2-(4-cyanophenyl)-2-oxoacetate

Product Name:methyl 2-(4-cyanophenyl)-2-oxoacetate

IUPAC Name:methyl 2-(4-cyanophenyl)-2-oxoacetate

: CAS：52798-47-7; Molecular Formula：C10H7NO3; Purity：95%

: Catalog Number：CM193809; Molecular Weight：189.17

Packing Unit	Available Stock	Price($)
CM193809-10g	3-4 Weeks	Źȃŉ
CM193809-25g	3-4 Weeks	Ɠǵŗ
CM193809-100g	3-4 Weeks	ƥƓǊů

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Product Details

: CAS NO:52798-47-7; Molecular Formula:C10H7NO3; Melting Point:-; Smiles Code:O=C(OC)C(C1=CC=C(C#N)C=C1)=O; Density:

: Catalog Number:CM193809; Molecular Weight:189.17; Boiling Point:; MDL No:; Storage:Store at 2-8°C.

Category Infos

: Benzenes; Benzene is an important organic compound with the chemical formula C6H6, and its molecule consists of a ring of 6 carbon atoms, each with 1 hydrogen atom. Benzene is a sweet, flammable, colorless and transparent liquid with carcinogenic toxicity at room temperature, and has a strong aromatic odor. It is insoluble in water, easily soluble in organic solvents, and can also be used as an organic solvent itself. The ring system of benzene is called benzene ring, and the structure after removing one hydrogen atom from the benzene ring is called phenyl. Benzene is one of the most important basic organic chemical raw materials. Many important chemical intermediates can be derived from benzene through substitution reaction, addition reaction and benzene ring cleavage reaction.

Product Other Information

Product Overview	methyl 2-(4-cyanophenyl)-2-oxoacetate, commonly known as Methyl Cyanoacetate, is an organic compound with the molecular formula C10H7NO3. It is a colorless to pale yellow liquid that is widely used in organic synthesis. Methyl Cyanoacetate is a versatile compound that has a wide range of applications in various fields, including pharmaceuticals, agrochemicals, and polymers.
Synthesis and Application	Methyl Cyanoacetate can be synthesized by the reaction of malonic acid diethyl ester with potassium cyanide, followed by esterification with methyl iodide. The reaction proceeds via a nucleophilic substitution mechanism, resulting in the formation of Methyl Cyanoacetate. Methyl Cyanoacetate has been extensively used in scientific research due to its versatile nature. It is used as a building block in the synthesis of various compounds, including pharmaceuticals, agrochemicals, and polymers. Methyl Cyanoacetate has been used in the synthesis of anti-tumor agents, anti-inflammatory agents, and anti-microbial agents. It has also been used in the synthesis of herbicides and insecticides.
Future Directions	There are several future directions for the use of Methyl Cyanoacetate in scientific research. It can be used in the synthesis of new anti-tumor agents, anti-inflammatory agents, and anti-microbial agents. It can also be used in the synthesis of new herbicides and insecticides. Further studies are needed to explore the biochemical and physiological effects of Methyl Cyanoacetate.