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1,2-Dihydro-1-phenyl-3H-naphtho[1,2-e][1,3]oxazin-3-one is a complex organic compound with the molecular formula C17H13NO2. It belongs to the class of naphtho[1,2-e][1,3]oxazine derivatives, which are heterocyclic compounds containing a benzene ring fused to an oxazine ring. This particular compound features a phenyl group attached to the naphthalene core, which is further fused with the oxazine ring. The compound is characterized by its unique chemical structure, which may exhibit various biological activities and potential applications in pharmaceuticals or materials science. Due to its complexity, further research and characterization are required to fully understand its properties and potential uses.

2911-24-2

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2911-24-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2911-24-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,1 and 1 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2911-24:
(6*2)+(5*9)+(4*1)+(3*1)+(2*2)+(1*4)=72
72 % 10 = 2
So 2911-24-2 is a valid CAS Registry Number.

2911-24-2Downstream Products

2911-24-2Relevant academic research and scientific papers

The effect of an N-heterocyclic compound on corrosion inhibition of J55 steel in sweet corrosive medium

Singh, Ambrish,Ansari,Quraishi,Kaya, Savas,Banerjee, Priyabrata

, p. 6303 - 6313 (2019)

The corrosion inhibition behavior of a naphthoxazinone derivative 1-phenyl-1,2-dihydronaphtho[1,2-e][1,3]oxazin-3-one (PNO) on J55 steel in 3.5 wt% NaCl solution saturated with carbon dioxide was evaluated using weight loss, electrochemical impedance spec

A novel three-component, one-pot synthesis of 1,2-dihydro-1-aryl-naphtho[1, 2-e][1,3]oxazine-3-one derivatives under microwave-assisted and thermal solvent-free conditions

Dabiri, Minoo,Delbari, Akram Sadat,Bazgir, Ayoob

, p. 821 - 823 (2007)

1,2-Dihydro-1-arylnaphtho[1,2-e][1,3]oxazine-3-one derivatives were synthesized in moderate to high yields using a novel, facile, and one-pot condensation of β-naphthol, aromatic aldehydes and urea under microwave-assisted and thermal solvent-free conditi

Bi-SO3H-functionalized room temperature ionic liquids based on bipyridinium: Highly efficient and recyclable catalysts for the synthesis of naphthalene-condensed oxazinone derivatives

Wang, Yuanyuan,Zhou, Junlong,Liu, Kun,Dai, Liyi

, p. 9965 - 9972 (2013)

Several bi-SO3H-functionalized room temperature ionic liquids were synthesized and their catalytic performances for the synthesis of naphthalene-condensed oxazinone derivatives were studied theoretically, as well as experimentally. Compared wit

Transformation reactions of the Betti base analog aminonaphthols

Szatmari, Istvan,Hetenyi, Anasztazia,Lazar, Laszlo,Fueloep, Ferenc

, p. 367 - 373 (2004)

By means of simple or domino ring-closure reactions of 1-(α- aminobenzyl)-2-naphthol (Betti base: 1), 1-aminomethyl-2-naphthol (2) and 2-(α-aminobenzyl)-1-naphthol (reverse Betti base: 3) with phosgene, ethyl benzimidate, 2-carboxybenzaldehyde, levulinic

Silica sulfuric acid catalyzed green synthesis of 1,2-dihydro-1-aryl naphtho[1,2-e][1,3]-oxazin-3-one and 1,2-dihydro-1-methyl naphtho[1,2-e][1,3]-oxazin-3-one as potent antibacterial agents

Imchen, Putusenla,Lensayula,Phucho, Tovishe,Thurr, Metsütu,Tumtin, Shokip,Zhimomi, Betokali K.

, p. 598 - 604 (2021/09/28)

A simple, efficient and green method for the preparation of naphthooxazinones employing easily available reagents 2-naphthol, aldehydes, urea and silica sulphuric acid (SSA) as catalyst is reported. The microwave assisted multi component reaction (MCR) pr

Synthesis, in vitro and in silico studies of naphto-1,3-oxazin-3(2H)-one derivatives as promising inhibitors of cholinesterase and α-glucosidase

Bendjeddou, Lamia,Bensouici, Chawki,Boudebbous, Khawla,Boulebd, Houssem,Debache, Abdelmadjid,Derabli, Chamseddine,Harakat, Dominique,Merazig, Hocine

, (2020/08/24)

Various substituted naphto-1,3-oxazin-3(2H)-one derivatives have been prepared by a three-component one-pot condensation reaction of 2-naphthol, aromatic aldehydes, and urea using phenylboronic acid as catalyst. The molecular structures of the synthesized

ompg-C3N4/SO3H organocatalyst-mediated green synthesis of 1,2-dihydro-1-arylnaphtho[1,2-e][1,3] oxazin-3-ones under solvent-free and mild conditions: a fast and facile one-pot three-component approach

Goodarzi, Nahal,Rashidizadeh, Afsaneh,Ghafuri, Hossein

, p. 791 - 798 (2020/05/14)

Abstract: In this research, we have described the synthesis of the well-ordered mesoporous graphite carbon nitride (ompg-C3N4) by applying SBA-15 as a potential hard silica template, and the catalytic performance of sulfonated well-o

Synthesis of dimeric pyridinium bromide under silica supported approach

Tamilarasan, Ramalingam,Govindaraj, Sadaiyan,Ganesan, Kilivelu

supporting information, p. 1190 - 1198 (2020/03/13)

Synthesis of dimeric substituted ester derivative of pyridinium salt with flexible linker units under conventional/silica supported approach. Solid-phase approach is much superior to the conventional method due to nontoxic, solvent free, easy work up proc

A one-pot multicomponent synthesis of naphthoxazin-3-one derivatives using amberlite IRA-400 Cl resin as green catalyst

Harichandran, Gurusamy,Parameswari, Parkunan,Shanmugam, Ponnusamy

, p. 600 - 605 (2018/06/26)

An efficient Amberlite IRA-400 Cl resin catalyzed, solvent-free, one-pot synthesis of 1- aryl-1,2-dihydro-3H-naphtho[1,2-e][1,3]oxazin-3-ones via three-component reaction of arylaldehydes, urea, and β-naphthol are described. This method offers advantages

A one-pot synthesis of 1,2-dihydro-1-arylnaphtho[1,2-e][1,3]oxazine-3-ones catalyzed by iron(III) phosphate under solvent-free condition

Rahmani, Parisa,Behbahani, Farahnaz K.

, p. 713 - 716 (2017/08/10)

An efficient green route for the preparation of naphthoxazinones, applying a three-component one-pot condensation reaction of 2-naphthol, aromatic aldehyde, and urea in the presence of iron(III) phosphate under solvent-free conditions, has been developed.

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