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2-(4-chlorophenyl)-2,3-dihydro-1H-naphtho[1,2-e][1,3]oxazine is a complex organic chemical compound with the molecular formula C17H13ClNO. It features a naphtho[1,2-e][1,3]oxazine core structure, which is a fused ring system consisting of a naphthalene and an oxazine ring. The compound is characterized by the presence of a 4-chlorophenyl group attached to the 2-position of the naphtho[1,2-e][1,3]oxazine core. This specific arrangement of atoms and functional groups gives the compound unique chemical and physical properties, which may be relevant in various applications, such as pharmaceuticals or materials science. The compound's structure and properties make it a potential candidate for further study and development in these fields.

6638-18-2

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6638-18-2 Usage

Organic compound

A compound primarily made up of carbon, hydrogen, and other elements such as oxygen, nitrogen, and chlorine in this case.

Member of the oxazine family

Belongs to a group of heterocyclic compounds characterized by a benzo-fused oxazine ring system.

Contains a naphthalene ring system

The compound has a fused ring structure derived from naphthalene, which consists of two six-membered aromatic rings.

Heterocyclic compound

The compound features at least two different elements in its ring structure, such as carbon, hydrogen, oxygen, and nitrogen.

Potential applications in pharmaceuticals

It may have possible uses in the development of medications due to its unique chemical structure and properties.

Chemical intermediate in the synthesis of other organic compounds

The compound can be used as a starting material or building block for the production of other organic compounds through chemical reactions.

Handle with care and follow proper safety protocols

Due to potential hazards associated with the compound, it is essential to take necessary precautions and follow safety guidelines when working with it.

Check Digit Verification of cas no

The CAS Registry Mumber 6638-18-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,3 and 8 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6638-18:
(6*6)+(5*6)+(4*3)+(3*8)+(2*1)+(1*8)=112
112 % 10 = 2
So 6638-18-2 is a valid CAS Registry Number.
InChI:InChI=1/C18H14ClNO/c19-14-6-8-15(9-7-14)20-11-17-16-4-2-1-3-13(16)5-10-18(17)21-12-20/h1-10H,11-12H2

6638-18-2Downstream Products

6638-18-2Relevant academic research and scientific papers

Gum arabic-OPO3H2as a new natural-based green catalyst for the one-pot pseudo-four-component synthesis of naphtho[1,2-: E] [1,3]oxazines

Bamoniri, Abdolahamid,Fatemeh Mirjalili, Bi Bi,Hosseinikhah, Sahar Saadat,Salehi, Naeimeh

, p. 40508 - 40513 (2020/11/18)

Gum arabic-OPO3H2 (GA-OPO3H2) as a unique natural-based green catalyst was synthesized by the reaction of phosphorus pentoxide with gum arabic. The structure and properties of the catalyst were studied via several analysis methods such as FT-IR, MAPPING, EDS, SEM, XRD, and TGA. The efficiency of the above-mentioned catalyst was investigated for the synthesis of naphtho-1,3-oxazines via a pseudo-four-component reaction of primary amines, formaldehyde, and 2-naphthol under the solvent-free grinding condition at room temperature using an electrical mortar-heater. The obtained results indicated that GA-OPO3H2 is a highly efficient green catalyst for the synthesis of naphtho[1,2-e][1,3]oxazines with high yields, simple workup, and benign reaction condition.

Nano-Fe3O4?walnut shell/Cu(ii) as a highly effective environmentally friendly catalyst for the one-potpseudothree-component synthesis of 1,3-oxazine derivatives under solvent-free conditions

Fatemeh Mirjalili, Bi Bi,Tafti, Arefeh Dehghani

, p. 31874 - 31880 (2020/09/21)

Fe3O4?walnut shell/Cu(ii) as an eco-friendly bio-based magnetic nano-catalyst was prepared by adding CuCl2to Fe3O4?walnut shell in alkaline medium. A series of 2-aryl/alkyl-2,3-dihydro-1H-naphtho[1,2-e][1,3]oxazines were synthesized by the one-potpseudothree-component reaction of β-naphthol, formaldehyde and various amines using nano-Fe3O4?walnut shell/Cu(ii) at 60 °C under solvent-free conditions. The catalyst was removed from the reaction mixture by an external magnet and was reusable several times without any considerable loss of its activity. This protocol has several advantages such as excellent yields, short reaction times, clean and convenient procedure, easy work-up and use of an eco-friendly catalyst.

Ultrasound-assisted one-pot synthesis of 1,3-oxazine derivatives catalysed by BF3-SiO2 under neat conditions

Reddy, Mudumala Veeranarayana,Lim, Kwon Taek,Kim, Jong Tae,Jeong, Yeon Tae

experimental part, p. 398 - 401 (2012/09/21)

An efficient and environment-friendly method for the synthesis of 1,3-oxazine derivatives has been developed using the ultrasound-mediated condensation of 2-naphthol with formaldehyde and primary amines under solvent-free condition at room temperature in

An eco-friendly synthesis and antimicrobial activities of dihydro-2H-benzo- and naphtho-1,3-oxazine derivatives

Mathew, Bijoy P.,Kumar, Awanit,Sharma, Satyasheel,Shukla,Nath, Mahendra

experimental part, p. 1502 - 1507 (2010/06/14)

A series of 3,4-dihydro-2H-benzo[e]-, 2,3-dihydro-1H-naphtho[1,2-e]-, 3,4-dihydro-2H-naphtho[2,1-e][1,3]oxazine and 1,2-bis(3,4-dihydrobenzo[e][1,3]oxazin-3(4H)-yl)ethane derivatives was obtained through an eco-friendly Mannich type condensation-cyclization reaction of phenols or naphthols with formaldehyde and primary amines in water at ambient temperature. Preliminary in vitro antimicrobial activity of the synthesized compounds was assessed against six pathogenic fungi, two Gram-negative and two Gram-positive bacteria. Some of the screened compounds have shown significant in vitro antimicrobial effect. Cytotoxic activities of the lead compounds (2m, 2n, 3c and 3d) against mouse fibroblast cell line (L929) were determined by MTT method. The assay results revealed that these molecules offered remarkable viability (>90%) of L929 cells at concentration of 25?μg/mL.

Heterocyclic spirocyclohexadienones, II

Mohrle,Schake

, p. 695 - 700 (2007/10/02)

Hofmann-Martius rearrangement of differently substituted aniline derivatives is investigated and the synthesis of spirocyclohexadienones 5 and 25 is performed. In comparison with 9, a N-aliphatic spiro compound, 5 and 25 give partially different reactions, the cause of which is discussed.

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