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1H-Naphth[2,3-d]imidazole-4,9-dione, 2-phenyl- is a complex organic compound with the molecular formula C16H9N2O2. It is a derivative of naphthimidazole, featuring a naphthalene ring fused with an imidazole ring, and a phenyl group attached to the 2-position. 1H-Naphth[2,3-d]imidazole-4,9-dione, 2-phenyl- is characterized by its unique structure, which includes a 1H-naphthoimidazole core with two carbonyl groups at the 4 and 9 positions, and a phenyl ring at the 2 position. It is known for its potential applications in the field of medicinal chemistry, particularly in the development of novel therapeutic agents. The compound's properties, such as its reactivity and stability, are influenced by the presence of the aromatic rings and the nitrogen atoms within its structure.

4496-29-1

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4496-29-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4496-29-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,9 and 6 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4496-29:
(6*4)+(5*4)+(4*9)+(3*6)+(2*2)+(1*9)=111
111 % 10 = 1
So 4496-29-1 is a valid CAS Registry Number.

4496-29-1Downstream Products

4496-29-1Relevant academic research and scientific papers

Synthesis of 2-aryl-1-hydroxy-1H-naphtho[2,3-d]imidazole-4,9-diones by reaction of 2-benzylamino-1,4-naphthoquinones with nitric acid

Gornostaev,Vigant,Kargina,Kuznetsova,Khalyavina, Yu. G.,Lavrikova

, p. 1354 - 1357 (2013)

2-Aryl-1-hydroxy-1H-naphtho[2,3-d]imidazole-4,9-diones were synthesized by treatment of 2-benzylamino-1,4-naphthoquinones with a mixture of nitric and sulfuric acids in acetic acid.

Micelles catalyzed one pot regio- and chemoselective synthesis of benzo[a]phenazines and naphtho[2,3-d]imidazoles 'in H2O'

Tandon, Vishnu K.,Verma, Manoj K.,Maurya, Hardesh K.,Kumar, Sandeep

, p. 6331 - 6334 (2014/12/10)

An efficient, novel, and concise one pot regio- and chemoselective synthesis of benzo[a]phenazines (4) and naphtho[2,3-d]imidazoles (8) has been accomplished in excellent yields by nucleophilic substitution reaction of 2,3-dichloro-1,4-naphthoquinone (1) with o-phenylenediamine (2) and benzamidines (7) respectively 'in H2O' using base and micelles (SDS) as catalyst. Analog reaction of 2,3-dichloro-1,4-naphthoquinone (1) with 2-aminobenzenethiol (9) under identical conditions led to formation of a mixture of benzo[b]phenothiazine (10), benzo[a]phenothiazine (11), and benzo[a]-1,4-benzothiazino-3,2-phenothiazine (12) in 17%, 23%, and 57% yields, respectively.

Tuning of the H-bonding ability of imidazole N-H towards the colorimetric sensing of fluoride and cyanide ions as their sodium salts in water

Manivannan, Ramalingam,Satheshkumar, Angupillai,Elango, Kuppanagounder P.

supporting information, p. 3152 - 3160 (2013/10/01)

Imidazole functionalized receptors, 2-R-1H-naphtho[2,3-d]imidazole-4,9- dione (2a-h), containing naphthoquinone as a chromogenic signalling unit have been synthesized from the reaction of 2,3-diaminonaphthoquinone and different aldehydes. These receptors

Facile synthesis of new imidazoles from direct reaction of 2,3-diamino-1,4-naphthoquinone with aldehydes

Aly, Ashraf A.,Hassan, Alaa A.,Brown, Alan B.,El-Shaieb, Kamal M.,Bedair, Tarek M. I.

experimental part, p. 787 - 791 (2011/09/16)

Figure represented. New imidazoles were easily prepared from 2,3-diamino-1,4-naphthoquinone and stoichiometric quantities of the appropriate aldehydes in dimethyl sulfoxide as a solvent. The reaction proceeded for few hours. The procedure can be generaliz

Use of tricyclic derivatives of 1,4-dihydro-1,4-dioxo-1H-naphthalene, novel compounds obtained and their application in theraphy

-

, (2008/06/13)

The invention concerns the therapeutic use of tricyclic salts and their pharmaceutically acceptable salts having the general formula: in which: A is either a sulfur atom, an oxygen atom, or an R3N radical where R3is a hydrogen atom,

Synthesis of 1,4-Diazepines

Krieg, Benno,Urban, Ralf

, p. 799 - 802 (2007/10/02)

2,3-Diamino-1,4-naphthoquinone (1) reacts with variously substituted derivatives of diethyl malonate (2,5, and 7) to yield the imidazole derivative 8, a tetraethyl tetracarboxylate of type 6, or substituted diaminonaphthoquinones 3.These react further in

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