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15448-59-6

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15448-59-6 Usage

Description

Naphth[2,3-b]oxirene-2,7-dione, 1a,7a-dihydro-1a-methyl(9CI) is a complex organic compound characterized by its unique molecular structure. It belongs to the class of naphthoquinones and is known for its potential applications in various fields due to its chemical properties.

Uses

Used in Pharmaceutical Industry:
Naphth[2,3-b]oxirene-2,7-dione, 1a,7a-dihydro-1a-methyl(9CI) is used as a pharmaceutical agent for its potential cytotoxic effects on tumor cells. It has been found to induce selective tumor cytotoxicity in neuroblastoma and other cancer cell lines, making it a promising candidate for cancer treatment.
Used in Anticancer Applications:
As an anticancer agent, Naphth[2,3-b]oxirene-2,7-dione, 1a,7a-dihydro-1a-methyl(9CI) is utilized for its ability to induce apoptosis through the activation of ROS-dependent ERK and JNK protein phosphorylation. This mechanism of action suggests its potential use in targeting cancer cells and promoting cell death, thereby contributing to tumor regression.
Used in Drug Delivery Systems:
Naphth[2,3-b]oxirene-2,7-dione, 1a,7a-dihydro-1a-methyl(9CI) can also be employed in the development of novel drug delivery systems to enhance its bioavailability and therapeutic outcomes. By incorporating this compound into various organic and metallic nanoparticles, its delivery to target cancer cells can be improved, leading to more effective treatment options.

Check Digit Verification of cas no

The CAS Registry Mumber 15448-59-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,4,4 and 8 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 15448-59:
(7*1)+(6*5)+(5*4)+(4*4)+(3*8)+(2*5)+(1*9)=116
116 % 10 = 6
So 15448-59-6 is a valid CAS Registry Number.
InChI:InChI=1/C11H8O3/c1-11-9(13)7-5-3-2-4-6(7)8(12)10(11)14-11/h2-5,10H,1H3

15448-59-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1a-methyl-7aH-naphtho[2,3-b]oxirene-2,7-dione

1.2 Other means of identification

Product number -
Other names 2,3-Epoxy-2,3-dihydro-2-methyl-1,4-naphthoquinone

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:15448-59-6 SDS

15448-59-6Relevant articles and documents

Fabrication, characterization and structure activity relationship of Co and Mn encapsulated on magnetic nanocomposite and its application in one-pot tandem synthesis of various tetrazoles and vitamin K3

Ashouri, Fatemeh,Farahanipour, Alireza,Faraji, Ali Reza,Hekmatian, Zahra

, (2022/02/21)

Considering the importance of vitamin K3 in commercial pet foods, veterinary medicines, poultry, and some swine feed and also tetrazole derivatives in pharmacy, medicine, chemistry, petroleum, and military industry, design efficient catalytic systems are desirable. Herein, four magnetic nanocomposites (MNCs) of cobalt and manganese using metformin, 3-aminopropyltrimethoxysilane (L1) and 2-aminoethyl-3-aminopropyltrimethoxysilane (L2) were designed and constructed as an efficient and controllable catalytic system. The synthesized nanocomposites fully characterized by FT-IR, AAS, ICP-OES, BET, CHN elemental analysis, SEM, TEM, DLS, EDX, TGA, VSM, and XPS spectroscopy. The well-prepared magnetically recoverable nanocomposites were used in the synthesis of a wide derivatives of α-hydrazino tetrazoles (α-HyT), ferrocenyltetrazoles (FcT), arylaminotetrazoles (ArAT) and also vitamin K3. Besides, the effect of operating parameters, such as the amount of catalyst, nature of solvent, temperature and reaction time, metal nature, chain length and hydrophobicity properties of linkers, was studied in the catalytic efficiency of synthesized nanocatalysts. The best catalytic results were obtained in the following order: FS-L2-Met@Co(II) > FS-L2-Met@Mn(II) > FS-L1-Met@Co(II) > FS-L1-Met@Mn(II) due to their structural characteristics. In addition to high TOF, these magnetic nanocomposites are superior in easy, inexpensive, and commercially preparation, keeping the structural and magnetic characteristics, easy magnetically separation from the reaction medium, short reaction time, mild reaction condition, easy work-up, and reusability without any metal leaching in six runs. Graphical abstract: [Figure not available: see fulltext.]

Tridentate 3-Substituted Naphthoquinone Ruthenium Arene Complexes: Synthesis, Characterization, Aqueous Behavior, and Theoretical and Biological Studies

Geisler, Heiko,Westermayr, Julia,Cseh, Klaudia,Wenisch, Dominik,Fuchs, Valentin,Harringer, Sophia,Plutzar, Sarah,Gajic, Natalie,Hejl, Michaela,Jakupec, Michael A.,Marquetand, Philipp,Kandioller, Wolfgang

, p. 9805 - 9819 (2021/06/30)

A series of nine RuII arene complexes bearing tridentate naphthoquinone-based N,O,O-ligands was synthesized and characterized. Aqueous stability and their hydrolysis mechanism were investigated via UV/vis photometry, HPLC-MS, and density functional theory calculations. Substituents with a positive inductive effect improved their stability at physiological pH (7.4) intensely, whereas substituents such as halogens accelerated hydrolysis and formation of dimeric pyrazolate and hydroxido bridged dimers. The observed cytotoxic profile is unusual, as complexes exhibited much higher cytotoxicity in SW480 colon cancer cells than in the broadly chemo- (incl. platinum-) sensitive CH1/PA-1 teratocarcinoma cells. This activity pattern as well as reduced or slightly enhanced ROS generation and the lack of DNA interactions indicate a mode of action different from established or previously investigated classes of metallodrugs.

Heterogeneous epoxidation of menadione with hydrogen peroxide over the zeolite imidazolate framework ZIF-8

Evtushok, Vasilii Yu.,Ivanchikova, Irina D.,Kholdeeva, Oxana A.,Kolokolov, Danil I.,Stepanov, Alexander G.,Zalomaeva, Olga V.

supporting information, p. 12546 - 12549 (2020/10/05)

The zeolite imidazolate framework ZIF-8 exhibits superior catalytic performance in the epoxidation of the electron-deficient CC bond in menadione using aqueous hydrogen peroxide as the oxidant. The catalysis has a truly heterogeneous nature and the framework structure remains intact. This is the first example of oxidation catalysis with ZIF-8.

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