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6-NITRO-1,2,3,4-TETRAHYDRO QUINOXALINE is a chemical compound characterized by the molecular formula C8H8N2O2. It is a nitro-substituted quinoxaline derivative known for its neuroprotective and anti-inflammatory properties. 6-NITRO-1,2,3,4-TETRAHYDRO QUINOXALINE is utilized in the synthesis of pharmaceuticals and other organic compounds, making it a significant component in the development of new drugs and materials.

41959-35-7

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41959-35-7 Usage

Uses

Used in Pharmaceutical Synthesis:
6-NITRO-1,2,3,4-TETRAHYDRO QUINOXALINE is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure and properties make it a valuable building block for the creation of new drugs with potential therapeutic applications.
Used in Neurodegenerative Disease Treatment:
In the field of medicine, 6-NITRO-1,2,3,4-TETRAHYDRO QUINOXALINE is used as a potential therapeutic agent for the treatment of neurodegenerative diseases. Its neuroprotective properties have been studied for their ability to protect neurons from damage and degeneration, offering hope for patients suffering from conditions such as Alzheimer's, Parkinson's, and multiple sclerosis.
Used in Inflammatory Condition Management:
6-NITRO-1,2,3,4-TETRAHYDRO QUINOXALINE is also used as an anti-inflammatory agent in the management of various inflammatory conditions. Its capacity to reduce inflammation and alleviate symptoms makes it a promising candidate for the development of new treatments for conditions such as arthritis, asthma, and inflammatory bowel disease.
Used in Organic Compound Synthesis:
In the chemical industry, 6-NITRO-1,2,3,4-TETRAHYDRO QUINOXALINE is used as a versatile building block in the synthesis of a wide range of organic compounds. Its reactivity and functional groups make it suitable for various chemical reactions, contributing to the creation of new materials and compounds with diverse applications.
Safety Precautions:
It is crucial to handle 6-NITRO-1,2,3,4-TETRAHYDRO QUINOXALINE with care, as it may pose health risks if ingested or inhaled. Proper safety measures, including the use of personal protective equipment and adherence to safety protocols, should be taken to minimize exposure and ensure the well-being of individuals working with this chemical compound.

Check Digit Verification of cas no

The CAS Registry Mumber 41959-35-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,9,5 and 9 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 41959-35:
(7*4)+(6*1)+(5*9)+(4*5)+(3*9)+(2*3)+(1*5)=137
137 % 10 = 7
So 41959-35-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H9N3O2/c12-11(13)6-1-2-7-8(5-6)10-4-3-9-7/h1-2,5,9-10H,3-4H2

41959-35-7SDS

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 6-nitro-1,2,3,4-tetrahydroquinoxaline

1.2 Other means of identification

Product number -
Other names 6-Nitro-1,2,3,4-tetrahydro-chinoxalin

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:41959-35-7 SDS

41959-35-7Downstream Products

41959-35-7Relevant academic research and scientific papers

Tetrabutylammonium Bromide-Catalyzed Transfer Hydrogenation of Quinoxaline with HBpin as a Hydrogen Source

Guo, Qi,Chen, Jingchao,Shen, Guoli,Lu, Guangfu,Yang, Xuemei,Tang, Yan,Zhu, Yuanbin,Wu, Shiyuan,Fan, Baomin

, p. 540 - 546 (2021/12/27)

A metal-free environmentally benign, simple, and efficient transfer hydrogenation process of quinoxaline has been developed using the HBpin reagent as a hydrogen source. This reaction is compatible with a variety of quinoxalines offering the desired tetrahydroquinoxalines in moderate-to-excellent yields with Bu4NBr as a noncorrosive and low-cost catalyst.

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