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(3E)-3-[2-(4-nitrophenyl)-2-oxoethylidene]-3,4-dihydroquinoxalin-2(1H)-one is a heterocyclic compound characterized by a quinoxaline ring and a nitrophenyl group. This organic compound holds potential in pharmaceuticals and agrochemicals due to its unique structure and functional groups.

66751-91-5

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66751-91-5 Usage

Uses

Used in Pharmaceutical Industry:
(3E)-3-[2-(4-nitrophenyl)-2-oxoethylidene]-3,4-dihydroquinoxalin-2(1H)-one is used as a precursor in the synthesis of new drugs for its heterocyclic structure, which may contribute to the development of pharmaceuticals with novel biological activities.
Used in Agrochemical Industry:
(3E)-3-[2-(4-nitrophenyl)-2-oxoethylidene]-3,4-dihydroquinoxalin-2(1H)-one is used as a potential active ingredient in agrochemicals, particularly as a pesticide or herbicide, due to the presence of the nitro group which may confer these properties.
Further studies are necessary to fully explore and understand the potential uses and effects of (3E)-3-[2-(4-nitrophenyl)-2-oxoethylidene]-3,4-dihydroquinoxalin-2(1H)-one in both industries.

Check Digit Verification of cas no

The CAS Registry Mumber 66751-91-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,7,5 and 1 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 66751-91:
(7*6)+(6*6)+(5*7)+(4*5)+(3*1)+(2*9)+(1*1)=155
155 % 10 = 5
So 66751-91-5 is a valid CAS Registry Number.

66751-91-5SDS

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 (3E)-3-[2-(4-nitrophenyl)-2-oxoethylidene]-1,4-dihydroquinoxalin-2-one

1.2 Other means of identification

Product number -
Other names -

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:66751-91-5 SDS

66751-91-5Relevant academic research and scientific papers

Five-Membered 2,3-Dioxo Heterocycles. XXXIX. Reaction of 4-Aroyl-1-aryl-5-methoxycarbonyl- and 1-Aryl-4-isopropyloxalo-5-phenyl-2,3-dihydropyrrole-2,3-diones with o-Phenylenediamine

Maslivets, A. N.,Smirnova, L. I.,Ivanenko, O. I.,Andreichikov, Yu. S.

, p. 563 - 568 (2007/10/03)

4-Aroyl-1-aryl-5-methoxycarbonyl- and 1-aryl-4-isopropyloxalo-5-phenyl-2,3-dihydropyrrole-2,3-diones react with p-phenylenediamine to give substituted 1,2,3,5,10,10a-hexahydropyrrolobenzodiazepine-2,3-diones.Hydrolysis of the latter yields 3-phenacylidene-1,2,3,4-tetrahydroquinoxalin-2-ones.

CHEMISTRY OF OXALYL DERIVATIVES OF METHYL KETONES. XXXV. KINETICS OF THE FORMATION OF 3-PHENACYLIDENE-3,4-DIHYDRO-2-QUINOXALONES FROM ARYLAMIDES OF AROYLPYRUVIC ACIDS AND o-PHENYLENEDIAMINE

Andreichikov, Yu.S.,Kozlov, A.P.,Kurdina, L.N.

, p. 752 - 756 (2007/10/02)

The kinetics of the acid-catalyzed reactions of the arylamides of aroylpyruvic acids with o-phenylenediamine, leading to the formation of 3-phenacylidene-2-quinoxalones, were investigated.It was established that the reaction rate is controlled by nucleophilic attack by the amide carbonyl at the cyclization stage.

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