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4-Methoxy-8-nitroquinoline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

89770-28-5

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89770-28-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89770-28-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,7,7 and 0 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 89770-28:
(7*8)+(6*9)+(5*7)+(4*7)+(3*0)+(2*2)+(1*8)=185
185 % 10 = 5
So 89770-28-5 is a valid CAS Registry Number.

89770-28-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Methoxy-8-nitroquinoline

1.2 Other means of identification

Product number -
Other names 4-methoxy-8-nitro-quinoline

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:89770-28-5 SDS

89770-28-5Downstream Products

89770-28-5Relevant academic research and scientific papers

Visible-Light-Photocatalyzed Reductions of N-Heterocyclic Nitroaryls to Anilines Utilizing Ascorbic Acid Reductant

Todorov, Aleksandar R.,Aikonen, Santeri,Muuronen, Mikko,Helaja, Juho

, p. 3764 - 3768 (2019/05/24)

A photoreductive protocol utilizing [Ru(bpy)3]2+ photocatalyst, blue light LEDs, and ascorbic acid (AscH2) has been developed to reduce nitro N-heteroaryls to the corresponding anilines. Based on experimental and computational results and previous studies, we propose that the reaction proceeds via proton-coupled electron transfer between AscH2, photocatalyst, and the nitro N-heteroaryl. The method offers a green catalytic procedure to reduce, e.g., 4-/8-nitroquinolines to the corresponding aminoquinolines, substructures present in important antimalarial drugs.

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