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Isoxazole, 4,5-dihydro-5-(1-naphthalenyl)-3-phenyl- is a complex organic compound with the molecular formula C20H17NO. It is a derivative of isoxazole, a heterocyclic compound containing a five-membered ring with one oxygen and one nitrogen atom. The compound features a 4,5-dihydro structure, which means it has two hydrogen atoms attached to the carbon atoms at positions 4 and 5 of the isoxazole ring. Additionally, it has a 1-naphthalenyl group attached to the 5-position and a phenyl group at the 3-position, both of which are aromatic rings. Isoxazole, 4,5-dihydro-5-(1-naphthalenyl)-3-phenyl- is of interest in organic chemistry and may have potential applications in the synthesis of pharmaceuticals and other specialty chemicals due to its unique structure and properties.

1035-92-3

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1035-92-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1035-92-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,3 and 5 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1035-92:
(6*1)+(5*0)+(4*3)+(3*5)+(2*9)+(1*2)=53
53 % 10 = 3
So 1035-92-3 is a valid CAS Registry Number.

1035-92-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-naphthalen-1-yl-3-phenyl-4,5-dihydro-isoxazole

1.2 Other means of identification

Product number -
Other names 5-Naphthalen-1-yl-3-phenyl-4,5-dihydro-isoxazole

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1035-92-3 SDS

1035-92-3Downstream Products

1035-92-3Relevant academic research and scientific papers

Anti-corrosive property of bioinspired environmental benign imidazole and isoxazoline heterocyclics: A cumulative studies of experimental and DFT methods

Ramkumar, Sowmya,Nalini,Quraishi, Mumtaz A.,Ebenso, Eno E.,Verma, Chandrabhan

, p. 103 - 119 (2020)

In the present study, four imidazoline (IDZ) and four isoxazolines (ISO) heterocyclics differing in the nature of methoxy (-OCH3) and aromatic (phenyl and naphthyl) moieties are synthesized, characterized and evaluated as corrosion inhibitors for mild steel in acidic solution of 1 M HCl. Results showed that imidazoline based heterocyclic compounds are better corrosion inhibitors than isoxazoline based heterocyclics and both classes of compounds showed inhibition efficiency of more than 85% at 20 mgL?1 concentration. Results further showed that inhibitors containing methoxy, phenyl, and naphthyl moieties showed higher protection efficiency as compared to the inhibitors without these moieties. PDP Study revealed that investigated IDZs and ISOs acted as mixed type inhibitors and their adsorption on the metallic surface followed the Langmuir adsorption isotherm model. All the experimental results were corroborated by density function theory (DFT) based quantum chemical calculations. Numerous DFT based indices calculated for neutral as well as protonated forms of the IDZs and ISOs in order to get better insight about metal-IDZs/ISOs interactions. Outcomes of the DFT analysis showed that protonated (cationic) form of the all the inhibitors are more strongly adsorbed on the metallic surface as compared to their neutral form.

Synthesis of Isoxazolines and Isoxazoles via Metal-Free Desulfitative Cyclization

Cheng, Jiaxin,Yang, Ze,Li, Yuansheng,Xi, Yulan,Sun, Qiu,He, Ling

, p. 2385 - 2393 (2018/05/28)

A novel, one-pot reaction for the synthesis of isoxazolines and isoxazoles is developed via a cascade process under metal-free conditions. The approach involves the formation of intramolecular C-N and C-O bonds and intermolecular C-C bonds from aromatic alkenes or alkynes and N -hydroxysulfonamides using hypervalent iodine(VII) and iodine as the oxidant. Activation of C-H and C-C bonds/construction of C-O bonds/elimination of SO 2 /C-N bond formation is achieved in sequence in the reaction system.

Insertion of Nitrogen Oxide and Nitrosonium Ion into the Cyclopropane Ring: A New Route to 2-Isoxazolines and its Mechanistic Studies

Mizuno, Kazuhiko,Ichinose, Nobuyuki,Tamai, Toshiyuki,Otsuji, Yoshio

, p. 4669 - 4675 (2007/10/02)

The 9,10-dicyanoanthracene (DCA)-sensitized photoreaction of 1,2-diarylcyclopropanes 1a-d in nitrogen oxide (NO)-saturated CH3CN afforded 3,5-diaryl-2-isoxazolines 2a-d in excellent yields.The reaction of 1a-d with NOBF4 or with a mixture of NO and O2 in

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