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2-(quinolin-6-yl)ethanol is a chemical compound with the molecular formula C14H13NO, featuring a quinoline ring and an ethanol group. It is an organic compound that has garnered interest due to its potential applications in pharmaceuticals, agrochemicals, and therapeutics, as well as its antioxidant properties.

227809-77-0

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227809-77-0 Usage

Uses

Used in Pharmaceutical Industry:
2-(quinolin-6-yl)ethanol is used as a synthetic intermediate for the development of various drugs, leveraging its unique chemical structure to contribute to the creation of novel medicinal compounds.
Used in Agrochemical Industry:
In the agrochemical sector, 2-(quinolin-6-yl)ethanol serves as a building block in the synthesis of pesticides, potentially enhancing crop protection and yield through its incorporation into new formulations.
Used in Therapeutic Applications:
2-(quinolin-6-yl)ethanol is studied for its potential therapeutic effects, particularly in the treatment of conditions such as cancer and neurodegenerative diseases, due to its interaction with biological targets and pathways implicated in these conditions.
Used in Antioxidant-based Skincare Products:
Capitalizing on its antioxidant properties, 2-(quinolin-6-yl)ethanol is considered for use in skincare products to protect the skin from oxidative stress and potentially reduce signs of aging or environmental damage.
The diverse applications of 2-(quinolin-6-yl)ethanol underscore its versatility and the ongoing research and development efforts aimed at harnessing its full potential across different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 227809-77-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,7,8,0 and 9 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 227809-77:
(8*2)+(7*2)+(6*7)+(5*8)+(4*0)+(3*9)+(2*7)+(1*7)=160
160 % 10 = 0
So 227809-77-0 is a valid CAS Registry Number.

227809-77-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-quinolin-6-ylethanol

1.2 Other means of identification

Product number -
Other names 6-Quinolineethanol

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:227809-77-0 SDS

227809-77-0Downstream Products

227809-77-0Relevant academic research and scientific papers

QUINSTATIN COMPOUNDS

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Page/Page column 76; 77, (2017/02/24)

The present disclosure relates to Quinstatin compounds, pharmaceutical compositions comprising such compounds, kits, and methods for using such compounds or pharmaceutical compositions.

Antineoplastic Agents. 603. Quinstatins: Exceptional Cancer Cell Growth Inhibitors

Pettit, George R.,Melody, Noeleen,Chapuis, Jean-Charles

, p. 692 - 698 (2017/04/01)

Discovery of the exceptionally powerful anticancer drug dolastatin 10 (1), contained in the sea hare Dolabella auricularia, opened a new frontier needed for improving human cancer treatment. Subsequently, major advances have been achieved based on results of structurally modifying this unusual natural peptide while maintaining the remarkable anticancer activity necessary for preparation of successful monoclonal antibody drug conjugates (ADC). Among the first several hundred SAR products based on dolastatin 10 our group synthesized and termed auristatins was auristatin E (2a). An anticancer activity-equivalent, desmethylaurisatin E (2b), linked to a CD30 monoclonal antibody is the very successful anticancer drug Adcetris, now approved for use in 65 countries. In the present investigation, we discovered a new subset of auristatins designated quinstatins derived from dolastatin 10 by replacing the C-terminal Doe unit with a carefully designed quinoline, which led to low or subnanomolar levels of cancer cell growth inhibition required for construction of chemically unique ADC drugs. The synthesis of quinstatins 2-8 is presented along with their cancer cell line biological data.

FUNCTIONALISED AND SUBSTITUTED INDOLES AS ANTI-CANCER AGENTS

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, (2016/02/05)

The present invention relates to anti-tropomyosin compounds, processes for their preparation, and methods for treating or preventing a disease or disorder, such as a proliferative disease (preferably cancer), using compounds of the invention.

NITROGEN-CONTAINING HETEROCYCLYL KETONES AND METHODS OF USE

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Page/Page column 167, (2008/12/08)

Selected compounds are effective for prophylaxis and treatment of diseases, such as HGF mediated diseases. The invention encompasses novel compounds, analogs, prodrugs and pharmaceutically acceptable salts thereof, pharmaceutical compositions and methods for prophylaxis and treatment of diseases and other maladies or conditions involving, cancer and the like. The subject invention also relates to processes for making such compounds as well as to intermediates useful in such processes.

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