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2-(quinazolin-4-ylamino)ethanol is a chemical compound with the molecular formula C11H11N3O, belonging to the class of quinazoline derivatives. It features both amino and alcohol functional groups, which contribute to its potential pharmacological properties. This versatile compound is recognized for its potential applications in the pharmaceutical industry, particularly in the synthesis of drugs and bioactive compounds, as well as in the development of novel organic compounds in laboratory settings.

5423-59-6

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5423-59-6 Usage

Uses

Used in Pharmaceutical Industry:
2-(quinazolin-4-ylamino)ethanol is used as a key intermediate in the synthesis of various drugs and bioactive compounds due to its unique chemical structure and pharmacological properties. Its presence in drug formulations is attributed to its potential to modulate biological activities, making it a valuable asset in medicinal chemistry.
Used in Medicinal Research:
2-(quinazolin-4-ylamino)ethanol is used as a research compound for exploring its anti-tumor and anti-inflammatory activities. Its potential in these areas positions it as a promising candidate for further investigation and development in the field of medicine, with the aim of identifying new therapeutic agents for the treatment of various diseases.
Used in Organic Synthesis:
In the laboratory, 2-(quinazolin-4-ylamino)ethanol is used as a building block for the synthesis of novel organic compounds. Its unique structure and functional groups make it a valuable component in the creation of new chemical entities with potential applications in various scientific and industrial fields.
Overall, 2-(quinazolin-4-ylamino)ethanol is a significant chemical compound with a broad spectrum of applications, particularly in the pharmaceutical and chemical synthesis sectors, where its unique properties are leveraged to develop innovative solutions and therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 5423-59-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,2 and 3 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5423-59:
(6*5)+(5*4)+(4*2)+(3*3)+(2*5)+(1*9)=86
86 % 10 = 6
So 5423-59-6 is a valid CAS Registry Number.

5423-59-6SDS

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 2-(quinazolin-4-ylamino)ethanol

1.2 Other means of identification

Product number -
Other names 2-quinazolin-4-ylamino-ethanol

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:5423-59-6 SDS

5423-59-6Downstream Products

5423-59-6Relevant academic research and scientific papers

A Mild and Regioselective Route to Functionalized Quinazolines

Maiden, Tracy M. M.,Swanson, Stephen,Procopiou, Panayiotis A.,Harrity, Joseph P. A.

supporting information, p. 14342 - 14346 (2015/10/05)

A Rh-catalyzed ortho-amidation cyclocondensation sequence gave a range of 4-aminoquinazolines in high yield. The method features a remarkably mild C(sp2)-H activation step and can be exploited to rapidly access compounds with established biological activity.

Synthesis of some nitrogen mustrads (Quinazoline series)

Sinha, Girish Kumar,Pandey, Bibhishan,Sinha, Alka

experimental part, p. 1401 - 1406 (2011/10/13)

Several nitrogen mustards with quinazoline moiety have been synthesised by condensation of 4-chloroquinazoline and 4,6- dichloroquinazoline with ethanol amine, diethanolamine and N-bis (2-chloroethyl) amine hydrochloride respectively.

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