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6-nitroquinoline-8-carboxylic acid is a chemical compound with the molecular formula C10H6N2O4, characterized by its yellow crystalline solid appearance. It is a versatile intermediate in the synthesis of pharmaceuticals and agrochemicals, known for its antimicrobial and antifungal properties, and is being explored for its potential in various applications across medicine, agriculture, and materials science.

70585-52-3

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70585-52-3 Usage

Uses

Used in Pharmaceutical Synthesis:
6-nitroquinoline-8-carboxylic acid is used as an intermediate in the pharmaceutical industry for the synthesis of various drugs. Its unique chemical structure and reactivity make it a valuable component in the development of new medicinal compounds.
Used in Agrochemical Synthesis:
In the agrochemical industry, 6-nitroquinoline-8-carboxylic acid is utilized as an intermediate for the production of pesticides and other agrochemicals. Its antimicrobial and antifungal properties contribute to the effectiveness of these products in protecting crops and managing pests.
Used in Antimicrobial Applications:
6-nitroquinoline-8-carboxylic acid is used as an antimicrobial agent for the treatment of various bacterial infections. Its ability to inhibit the growth of bacteria makes it a potential candidate for use in medical treatments and as a preservative in various products.
Used in Antifungal Applications:
6-nitroquinoline-8-carboxylic acid is also used as an antifungal agent, helping to combat fungal infections. Its application in this area can be beneficial in both medical and agricultural contexts, protecting both human health and crop yields.
Used in Organic Chemistry:
6-nitroquinoline-8-carboxylic acid is used as a building block in the synthesis of various organic compounds. Its versatile reactivity is a valuable asset in the field of organic chemistry, enabling the creation of a wide range of chemical products.
Used in Fluorescent Probes for Metal Ion Detection:
6-nitroquinoline-8-carboxylic acid has been investigated for its potential use as a fluorescent probe for detecting metal ions in biological systems. This application could be particularly useful in environmental monitoring, medical diagnostics, and materials science for the sensitive and selective detection of metal ions.

Check Digit Verification of cas no

The CAS Registry Mumber 70585-52-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,5,8 and 5 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 70585-52:
(7*7)+(6*0)+(5*5)+(4*8)+(3*5)+(2*5)+(1*2)=133
133 % 10 = 3
So 70585-52-3 is a valid CAS Registry Number.

70585-52-3SDS

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 6-nitroquinoline-8-carboxylic acid

1.2 Other means of identification

Product number -
Other names 8-Carboxy-6-nitroquinoline

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:70585-52-3 SDS

70585-52-3Downstream Products

70585-52-3Relevant academic research and scientific papers

Carbapenem antibiotic compounds

-

, (2008/06/13)

The present invention relates to carbapenems and provides a compound of the formula (I) STR1 wherein: R1 is 1-hydroxyethyl, 1-fluoroethyl or hydroxymethyl; R2 is hydrogen or C1-4 alkyl; R3 is hydrogen or C1-4 alkyl; P1 is of the formula: STR2 and one or two of A,B,C,D,E,F,G and H, are nitrogen and the remainder are CH; and P is bonded to the nitrogen of the linking carbamoyl group by a carbon atom, in either ring, is substituted by the carboxy group on a carbon atom, in either ring, and is optionally further substituted, by up to three substitutents, on a carbon atom, in either ring; or a pharmaceutically acceptable salt or in vivo hydrolysable ester thereof. Processes for their preparation, intermediates in their preparation, their use as therapeutic agents and pharmaceutical compositions containing them are also described.

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