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1,2-Ethanediamine, N,N'-bis(4-chlorophenyl)-1,2-diphenyl- is a complex organic compound with the chemical formula C20H18Cl2N2. It is a derivative of 1,2-ethanediamine, featuring two 4-chlorophenyl groups attached to the nitrogen atoms and two phenyl groups attached to the carbon atoms. 1,2-Ethanediamine, N,N'-bis(4-chlorophenyl)-1,2-diphenyl- is characterized by its symmetrical structure and the presence of two amine groups, which can participate in various chemical reactions, such as forming salts or coordination compounds. It is often used in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals due to its unique reactivity and structural properties.

2948-39-2

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2948-39-2 Usage

Explanation

The full chemical name of the compound, which describes its structure and composition.

Explanation

The compound belongs to a group of chemical compounds known as diphenylamines, which are characterized by having two phenyl groups attached to a nitrogen atom.

Explanation

The compound is also known by the trade name Chimassorb 944, which is a specific brand or product name for this chemical.

Explanation

The compound is commonly used as a stabilizer in the plastics and polymers industry to prevent degradation caused by ultraviolet radiation.

Explanation

The compound appears as a white to pale yellow powder, which is its solid form.

Explanation

The compound is soluble in organic solvents, such as alcohols, ethers, and hydrocarbons, but it does not dissolve in water.

Explanation

Ingesting the compound can be harmful or toxic to humans, and it should be handled with care to avoid accidental ingestion.

Explanation

Direct contact with the compound can cause irritation to the skin and eyes, so proper protective measures should be taken when handling it.

Class

Diphenylamines

Application

Stabilizer in plastics and polymers

Physical State

White to pale yellow powder

Solubility

Soluble in organic solvents, insoluble in water

Toxicity

Toxic if ingested

Skin and Eye Irritation

Can cause skin and eye irritation upon contact

Check Digit Verification of cas no

The CAS Registry Mumber 2948-39-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,4 and 8 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2948-39:
(6*2)+(5*9)+(4*4)+(3*8)+(2*3)+(1*9)=112
112 % 10 = 2
So 2948-39-2 is a valid CAS Registry Number.

2948-39-2Relevant articles and documents

Highly chemoselective crossed imino pinacol coupling reaction using the synergetic effect of boron trifluoride etherate and trichloromethylsilane

Shimizu, Makoto,Suzuki, Ikuhiro,Makino, Hiroaki

, p. 1635 - 1638 (2007/10/03)

Use of boron trifluoride etherate and trichloromethylsilane in the presence of zinc-copper couple effects a crossed imino pinacol coupling reaction to give 1,2-diamines in good yields with high diastereoselectivities.

Samarium Diiodide-Promoted Reductive Coupling of Imines

Imamoto, Tsuneo,Nishimura, Seijiro

, p. 1141 - 1142 (2007/10/02)

Aromatic aldimines are reductively coupled to 1,2-diamines by treatment with samarium diiodide.Cross-coupling of aromatic ketimines with ketones to 2-aminoalcohols is also promoted by the same reagent.

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