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90323-30-1

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90323-30-1 Usage

General Description

1-Methyl-6-nitro-1,2,3,4-tetrahydroquinoxaline-2,3-dione is a chemical compound with the molecular formula C9H9N3O4. It is a nitro-substituted quinoxaline derivative and it has a yellow crystalline appearance. 1-Methyl-6-nitro-1,2,3,4-tetrahydroquinoxaline-2,3-dione is known to have biological activity, specifically as an inhibitor of certain enzymes such as nitric oxide synthase. It has also been studied for its potential as a pharmaceutical agent, particularly in the treatment of neurodegenerative diseases and other conditions involving the central nervous system. Additionally, it has shown potential as a precursor for the synthesis of other organic compounds with various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 90323-30-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,3,2 and 3 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 90323-30:
(7*9)+(6*0)+(5*3)+(4*2)+(3*3)+(2*3)+(1*0)=101
101 % 10 = 1
So 90323-30-1 is a valid CAS Registry Number.

90323-30-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methyl-7-nitro-1H-quinoxaline-2,3-dione

1.2 Other means of identification

Product number -
Other names 1-methyl-6-nitroquinoxaline-2,3(1H,4H)-dione

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:90323-30-1 SDS

90323-30-1Downstream Products

90323-30-1Relevant articles and documents

Green synthesis method of N-substituted-1,4-dihydro-2,3-quinoxalinedione compound

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Paragraph 0044-0061; 0091-0094, (2020/01/12)

The invention discloses a green synthesis method of an N-substituted-1,4-dihydro-2,3-quinoxalinedione compound. The green synthesis method comprises the following steps: reacting ammonium persulfate with an N-substituted quinoxaline-2(1H)-one derivative in an aqueous solution of DL-alpha-tocopherol methoxy polyethylene glycol succinic acid water to generate the N-substituted-1,4-dihydro-2,3-quinoxalinedione compound; and after the reaction is finished, extracting a reaction product by using ethyl acetate, and performing vacuum drying to obtain the high-purity target product. The aqueous solution of the DL-alpha-tocopherol methoxy polyethylene glycol succinic acid can be recycled at least five times or more. The method is good in product selectivity, high in yield, simple in separation process, low in raw material cost, friendly to environment and beneficial for industrial production and application.

Synthesis and in vitro and in vivo biological evaluation of substituted nitroquinoxalin-2-ones and 2,3-diones as novel trichomonacidal agents

Ibá?ez-Escribano, Alexandra,Reviriego, Felipe,Nogal-Ruiz, Juan José,Meneses-Marcel, Alfredo,Gómez-Barrio, Alicia,Escario, José Antonio,Arán, Vicente J.

, p. 276 - 283 (2015/03/30)

Two series of ten novel 7-nitroquinoxalin-2-ones and ten 6-nitroquinoxaline-2,3-diones with diverse substituents at positions 1 and 4 were synthesized and evaluated against the sexually transmitted parasite Trichomonas vaginalis. Furthermore, diverse mole

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