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7-N-PROPYL-8-HYDROXYQUINOLINE is a chemical compound that belongs to the class of organic compounds known as hydroxyquinolines. These compounds contain a quinoline moiety, which is a bicyclic compound with a benzene ring fused to a pyridine ring, substituted by one hydroxyl group. The 7-N-PROPYL-8-HYDROXYQUINOLINE, specifically, has a propyl group attached to the nitrogen atom at the 7th position and a hydroxyl group at the 8th position of the quinoline ring. It is relatively lesser-known, and data regarding its exact uses, properties, and health effects are not extensively documented. However, quinolines and their derivatives are generally known for their bactericidal, antiseptic, and disinfectant properties.

58327-60-9

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58327-60-9 Usage

Uses

Used in Pharmaceutical Industry:
7-N-PROPYL-8-HYDROXYQUINOLINE is used as a potential pharmaceutical compound for its bactericidal, antiseptic, and disinfectant properties. These properties make it a candidate for the development of new drugs and treatments, particularly in the context of combating bacterial infections.
Used in Chemical Research:
7-N-PROPYL-8-HYDROXYQUINOLINE is used as a research compound in the field of organic chemistry. Its unique structure and properties make it an interesting subject for studies on the synthesis, reactivity, and potential applications of hydroxyquinoline derivatives.
Used in Material Science:
7-N-PROPYL-8-HYDROXYQUINOLINE is used as a component in the development of new materials, such as coatings or films, that may benefit from its antimicrobial properties. This could be particularly relevant in applications where preventing the growth of bacteria is crucial, such as in medical devices or food packaging.
Used in Environmental Applications:
7-N-PROPYL-8-HYDROXYQUINOLINE is used as an environmental agent for its potential to control microbial growth in various settings, such as water treatment or industrial processes. Its bactericidal properties could contribute to maintaining cleanliness and preventing the spread of harmful microorganisms.

Check Digit Verification of cas no

The CAS Registry Mumber 58327-60-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,3,2 and 7 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 58327-60:
(7*5)+(6*8)+(5*3)+(4*2)+(3*7)+(2*6)+(1*0)=139
139 % 10 = 9
So 58327-60-9 is a valid CAS Registry Number.

58327-60-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 8-Hydroxy-7-propylquinoline

1.2 Other means of identification

Product number -
Other names 7-propylquinolin-8-ol

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:58327-60-9 SDS

58327-60-9Upstream product

58327-60-9Downstream Products

58327-60-9Relevant academic research and scientific papers

Two-chamber hydrogen generation and application: Access to pressurized deuterium gas

Modvig, Amalie,Andersen, Thomas L.,Taaning, Rolf H.,Lindhardt, Anders T.,Skrydstrup, Troels

, p. 5861 - 5868 (2014/07/08)

Hydrogen and deuterium gas were produced and directly applied in a two-chamber system. These gaseous reagents were generated by the simple reaction of metallic zinc with HCl in water for H2 and DCl in deuterated water for D2. The setup proved efficient in classical Pd-catalyzed reductions of ketones, alkynes, alkenes, etc. in near-quantitative yields. The method was extended to the synthesis and isotope labeling of quinoline and 1,2,3,4-tetrahydroquinoline derivatives. Finally, CX-546 and Olaparib underwent efficient Ir-catalyzed hydrogen isotope exchange reactions.

Endothelin receptor antagonists

-

, (2008/06/13)

Novel compounds of the formula I STR1 in which R 1, R 2, R 3 and X have the meaning indicated in claim 1, and their salts exhibit endothelin receptor-antagonistic properties.

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