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1-Anthracenamine, N-(phenylmethylene)-, also known as N-(phenylmethylene)-1-anthracenamine or 1-(phenylmethylidene)-9-aminoanthracene, is an organic compound with the chemical formula C19H15N. It is a derivative of anthracene, a tricyclic aromatic hydrocarbon, with an amine group (-NH2) at the 1-position and a phenylmethylene group (-C6H5-CH=) attached to the nitrogen atom. 1-Anthracenamine, N-(phenylmethylene)- is characterized by its yellow crystalline appearance and is soluble in organic solvents such as ethanol and acetone. It is primarily used as a chemical intermediate in the synthesis of various dyes, pigments, and pharmaceuticals, owing to its unique chemical structure and properties.

899-77-4

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899-77-4 Usage

Derivative of Anthracene

Yes
It is derived from the parent compound anthracene, which is a polycyclic aromatic hydrocarbon.

Class of Compounds

Aminoanthracenes
It belongs to a group of organic compounds that contain an anthracene core with an amino group attached.

Primary Uses

Manufacturing of dyes and pigments
Production of organic semiconductors
Production of organic light-emitting diodes (OLEDs)

Potential Application

Photodynamic therapy for cancer treatment
It has been studied for its possible use in treating cancer through a non-invasive therapeutic approach.

Toxicity

Known to be toxic
The compound is toxic and should be handled with caution to avoid adverse health effects.

Check Digit Verification of cas no

The CAS Registry Mumber 899-77-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,9 and 9 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 899-77:
(5*8)+(4*9)+(3*9)+(2*7)+(1*7)=124
124 % 10 = 4
So 899-77-4 is a valid CAS Registry Number.

899-77-4Downstream Products

899-77-4Relevant academic research and scientific papers

Stereocontrolled synthesis of anticancer β-lactams via the Staudinger reaction

Banik, Bimal K.,Banik, Indrani,Becker, Frederick F.

, p. 3611 - 3622 (2007/10/03)

Stereocontrolled synthesis of novel β-lactams using polyaromatic imines following the Staudinger reaction has been accomplished. The effects of domestic microwave irradiation on this type of reaction have been investigated. Formation of trans-β-lactams has been explained through isomerization of the enolates formed during the reaction of acid chloride (equivalent) with imines in the presence of triethylamine. A donor-acceptor complex pathway is believed to be involved in the formation of cis-β-lactams. The effect of a peri hydrogen has been found to be significant in controlling the stereochemistry of the resulting β-lactams. SAR has identified β-lactams with anticancer activity. The presence of an acetoxy group has proven obligatory for their anticancer activity.

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