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2,3-DIPHENYL-QUINOXALINE-6-CARBOXYLIC ACID is an organic compound with a unique chemical structure, characterized by its greenish solid appearance. It possesses potential antineoplastic properties, making it a promising candidate for various applications in the pharmaceutical and medical industries.

32387-96-5

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32387-96-5 Usage

Uses

Used in Pharmaceutical Industry:
2,3-DIPHENYL-QUINOXALINE-6-CARBOXYLIC ACID is used as a potential antineoplastic agent for its ability to target and inhibit the growth of cancer cells. Its chemical properties allow it to interfere with essential cellular processes, thereby exhibiting potential therapeutic effects against various types of cancer.
Used in Research and Development:
In the field of research and development, 2,3-DIPHENYL-QUINOXALINE-6-CARBOXYLIC ACID serves as a valuable compound for studying its antineoplastic properties and exploring its potential applications in the development of novel cancer treatments. Its unique chemical structure provides a foundation for further investigation and modification to enhance its efficacy and selectivity towards cancer cells.
Used in Drug Design and Synthesis:
2,3-DIPHENYL-QUINOXALINE-6-CARBOXYLIC ACID can be utilized as a key building block or starting material in the design and synthesis of new antineoplastic drugs. Its chemical properties and potential antineoplastic activity make it an attractive candidate for the development of innovative therapeutic agents targeting cancer cells.

Check Digit Verification of cas no

The CAS Registry Mumber 32387-96-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,3,8 and 7 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 32387-96:
(7*3)+(6*2)+(5*3)+(4*8)+(3*7)+(2*9)+(1*6)=125
125 % 10 = 5
So 32387-96-5 is a valid CAS Registry Number.
InChI:InChI=1/C21H14N2O2/c24-21(25)16-11-12-17-18(13-16)23-20(15-9-5-2-6-10-15)19(22-17)14-7-3-1-4-8-14/h1-13H,(H,24,25)

32387-96-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-diphenylquinoxaline-6-carboxylic acid

1.2 Other means of identification

Product number -
Other names 2,3-Diphenyl-quinoxaline-6-carboxylic acid

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:32387-96-5 SDS

32387-96-5Relevant academic research and scientific papers

New quinoxalin-1,3,4-oxadiazole derivatives: Synthesis, characterization, in vitro biological evaluations, and molecular modeling studies

Mirzazadeh, Roghieh,Asgari, Mohammad S.,Barzegari, Ebrahim,Pedrood, Keyvan,Mohammadi-Khanaposhtani, Maryam,Sherafati, Maedeh,Larijani, Bagher,Rastegar, Hossein,Rahmani, Hojjat,Mahdavi, Mohammad,Taslimi, Parham,Eda M.,Gul?in, ?lhami

, (2021/05/19)

A new series of quinoxalin-1,3,4-oxadiazole (10a–l) derivatives was synthesized and evaluated against some metabolic enzymes including human carbonic anhydrase (hCA) isoenzymes I and II (carbonic anhydrases I and II), cholinesterase (acetylcholinesterase

HBTU-catalyzed simple and mild protocol for the synthesis of quinoxaline derivatives

Bhushan, B. Popatkar,Gangadhar, A. Meshram

, (2020/07/21)

HBTU-catalyzed, simple, mild, and effective protocol for the synthesis of quinoxalines has been established. The reaction between 1,2-diamines, benzil, and catalytic amount of HBTU in ethanol resulted into quinoxalines. Various aliphatic, aromatic and het

Triketone compound containing quinoxaline structure, and preparation method and application thereof

-

Paragraph 0101-0103, (2020/03/13)

The invention belongs to the technical field of medicine synthesis, and particularly relates to a triketone compound containing a quinoxaline structure, and a preparation method and an application thereof. The quinoxaline-containing triketone compound has a structure represented by general formula (I). The preparation method is mainly characterized in that a compound with a structure represented by formula (II) is contacted in the presence of an alkali and a solvent, and R1, R2, R3 and R4 in the formulas are respectively defined in the description. The quinoxaline-containing triketone compoundhas high herbicidal activity, and especially has an excellent effect of preventing and controlling broadleaf weeds and/or gramineous weeds, and the prevention and control effect is even better than that of some commercial herbicides sold in the market.

COMPOSITIONS AND METHODS OF MODULATING SHORT-CHAIN DEHYDROGENASE ACTIVITY

-

Paragraph 00480, (2018/08/26)

Compounds and methods of modulating 15-PGDH activity, modulating tissue prostaglandin levels, treating disease, diseases disorders, or conditions in which it is desired to modulate 15-PGDH activity and/or prostaglandin levels include 15-PGDH inhibitors de

A NOVEL QUINOXALINE COMPOUND FOR ULTRAVIOLET ABSORBERS

-

Paragraph 0087-0089; 0111-0113, (2017/10/21)

PURPOSE: A novel quinoxaline compound, isomer thereof, precursor drug thereof, or pharmaceutically acceptable salt thereof is provided to absorb UVA and UVB. CONSTITUTION: A quinoxaline compound is denoted by chemical formula 1. An UV absorber or pharmaceutical or cosmetic composition for antiaging contains the quinoxaline compound, isomer thereof, precursor drug thereof, or pharmaceutically acceptable salt, hydrate, or solvate thereof as an active ingredient.

Catalytic application of recyclable silica-supported bismuth(III) chloride in the benzo[N,N]-heterocyclic condensation

Aghapoor, Kioumars,Mohsenzadeh, Farshid,Shakeri, Atena,Darabi, Hossein Reza,Ghassemzadeh, Mitra,Neumüller, Bernhard

, p. 170 - 178 (2013/10/08)

Silica-supported bismuth(III) chloride (BiCl3/SiO2) has been successfully employed in the condensation of 1,2-dicarbonyls with a variety of arene-1,2-diamines bearing either electron withdrawing or donating functional groups. The catalyzed reaction proceeded smoothly under ambient temperature in methanol to give the corresponding quinoxaline and pyrido[2,3-b]pyrazine compounds in good to excellent yields. The catalyst exhibited remarkable reusable activity and higher catalytic performance than homogeneous BiCl3. A plausible mechanism for the catalytic action of BiCl3/SiO2 has been introduced. Moreover, the crystal structure of the prepared unsymmetrical benzo[N,N]-heterocycles has been determined by single crystal X-ray diffraction.

A recyclable solid acid catalyst sulfated titania for easy synthesis of quinoxaline and dipyridophenazine derivatives under microwave irradiation

Krishnakumar, Balu,Swaminathan, Meenakshisundaram

experimental part, p. 1261 - 1266 (2012/01/31)

TiO2SO42, prepared by solgel method has been used for the synthesis of quinoxaline and dipyridophenizine derivatives under microwave irradiation. High-resolution transmission electron microscope (HR-TEM) and atomic force m

Solvent free synthesis of quinoxalines, dipyridophenazines and chalcones under microwave irradiation with sulfated Degussa titania as a novel solid acid catalyst

Krishnakumar,Swaminathan

experimental part, p. 16 - 25 (2011/12/14)

Sulfated TiO2-P25 (Degussa titania) has been prepared by sol-gel method using H2SO4 and characterized by FT-IR, XRD, FE-SEM, EDS, HR-TEM, XPS, DRS and BET surface area measurements. Sulfate loading by H2SO4 increases the Lewis acidity of Degussa tiatania. This catalyst gives an excellent yield with less reaction time and is an inexpensive and easily recyclable solid acid catalyst for the synthesis of quinaxalines, dipyridophenazines and chalcones under microwave irradiation.

An efficient protocol for the green synthesis of quinoxaline and dipyridophenazine derivatives at room temperature using sulfated titania

Krishnakumar,Velmurugan,Jothivel,Swaminathan

experimental part, p. 997 - 1002 (2010/10/03)

Biologically active quinoxalines and dipyridophenazines were efficiently synthesized in excellent yield and less reaction time using inexpensive, easily recyclable sulfated titania (TiO2-SO42-). TiO2-SO42-

A recyclable and highly effective sulfated TiO2-P25 for the synthesis of quinoxaline and dipyridophenazine derivatives at room temperature

Krishnakumar,Swaminathan

experimental part, p. 2572 - 2577 (2010/11/18)

Sulfated TiO2-P25 has been prepared using H2SO 4 and used for the synthesis of quinoxaline and dipyridophenazine derivatives. Sulfate loading by H2SO4 increases the Lewis acidity of TiO2-P2

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