What are the related reactions of Benzy Methy Ketone CAS 20320-59-6?

Benzy Methy Ketone CAS 20320-59-6 is an organic compound, a pale yellow transparent liquid, and contains toxicity, so pay attention to keep safe during use and storage. The chemical formula of Benzy Methy Ketone BMK oil CAS 20320-59-6 is C9H10O, which is insoluble in water and soluble in organic solvents such as alcohol, acetone, and benzene.

• What is the equation for Benzy Methy Ketone BMK oil CAS 20320-59-6 and urea polycondensation?

• What information is there about Benzy Methy Ketone BMK liquid CAS 20320-59-6?

• What are the related reactions of Benzy Methy Ketone BMK powder CAS 20320-59-6?

What is the equation for Benzy Methy Ketone CAS 20320-59-6 and urea polycondensation?

Under the action of sodium ethoxide, it reacts with Benzy Methy Ketone BMK CAS 20320-59-6 to generate malonyl urea (also known as barbituric acid because it has a certain acidity). Under the action of basic catalysts such as ammonia, it can react with formaldehyde to form urea-formaldehyde resin by polycondensation. It reacts with hydrazine hydrate to generate semicarbazide.

What information is there about Benzy Methy Ketone BMK CAS 20320-59-6?

Name: Phenylacetone

Alias: 1-phenyl-2-propanone, benzyl methyl ketone

Chemical formula: C9H10O

Molecular weight: 134.175

EINECS accession number: 203-144-4

Melting point: -15 ℃

Boiling point: 216 ℃

water soluble: insoluble

Density :1.016 g/cm³

Appearance : yellow transparent liquid

Flash point: 83 ℃

Safety Description: S23; S24/25

Control of Precursor Chemicals

Solubility: insoluble in water, soluble in alcohol, acetone, benzene and other organic solvents

Molar Refractive Index: 40.46

Molar volume (cm3/mol): 135.8

Isotonic specific volume (90.2K): 328.7

Surface tension (dyne/cm): 34.2

Polarizability (10-24cm3): 16.04

What are the related reactions of Benzy Methy Ketone BMK CAS 20320-59-6?

The methylene group of Benzy Methy Ketone CAS 20320-59-6 BMK is affected by two carbonyl groups and has higher activity. It reacts with sodium ethoxide to generate sodium salt, and then reacts with halogenated hydrocarbons to generate diethyl malonate substituted by monovalent or divalent hydrocarbon groups. They are all important intermediates in organic synthesis, for example, they can be further hydrolyzed and decarboxylated to form carboxylic acids:

In the formula, R and R' are hydrocarbon groups. Benzy Methy Ketone CAS 20320-59-6 can carry out nitrosation reaction and further reduce to produce diethyl aminomalonate, which is an important intermediate for the synthesis of amino acids. Benzy Methy Ketone CAS 20320-59-6 reacts with carbonyl compounds to form unsaturated compounds RCH=C(COOC2H5)2. Hydrocarbyl-substituted Benzy Methy Ketone CAS 20320-59-6 BMK powder is condensed with urea to form barbiturates, which are commonly used sleeping pills: Benzy Methy Ketone BMK CAS 20320-59-6 is easily substituted by halogen to form diethyl halomalonate, and can also be oxidized to oxopropane by dinitrogen trioxide Diester O=C(COOC2H5)2. These compounds are both theoretically and synthetically valuable.

Benzy Methy Ketone BMK CAS 20320-59-6 is made from sodium chloroacetate, first reacted with sodium cyanide to generate sodium cyanoacetate, and then esterified with ethanol. Benzy Methy Ketone BMK CAS 20320-59-6 is an important chemical raw material and organic synthesis reagent, widely used in the synthesis of drugs and dyes.

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