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2-Chloro-6-ethyl-5-fluoro-4-hydroxy pyrimidine ammonium salt is a chemical compound characterized by a pyrimidine ring with a chloro, ethyl, fluoro, and hydroxy group attached to it, along with an ammonium salt. This versatile compound is known for its potential medicinal properties and is widely used in the pharmaceutical and research industries.

188416-27-5

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188416-27-5 Usage

Uses

Used in Pharmaceutical Synthesis:
2-Chloro-6-ethyl-5-fluoro-4-hydroxy pyrimidine ammonium salt is used as an intermediate in the synthesis of pharmaceuticals and other organic compounds. Its unique structure and functional groups make it a valuable building block for the development of new drugs and therapeutic agents.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, 2-Chloro-6-ethyl-5-fluoro-4-hydroxy pyrimidine ammonium salt is used for research and development purposes. Its potential medicinal properties are often studied for the treatment of various diseases and conditions, making it a promising candidate for drug discovery and optimization.
Used in Drug Design and Optimization:
The unique structure and functional groups of 2-Chloro-6-ethyl-5-fluoro-4-hydroxy pyrimidine ammonium salt make it a valuable tool in drug design and optimization. Researchers can modify its structure to create new compounds with improved pharmacological properties, such as increased potency, selectivity, and reduced side effects.
Used in Drug Delivery Systems:
2-Chloro-6-ethyl-5-fluoro-4-hydroxy pyrimidine ammonium salt can also be used in the development of drug delivery systems. Its chemical properties can be exploited to improve the solubility, stability, and bioavailability of therapeutic agents, leading to more effective treatments.
Overall, 2-Chloro-6-ethyl-5-fluoro-4-hydroxy pyrimidine ammonium salt is a versatile and valuable compound in the pharmaceutical and research industries, with a wide range of applications in drug synthesis, medicinal chemistry research, drug design and optimization, and drug delivery systems.

Check Digit Verification of cas no

The CAS Registry Mumber 188416-27-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,8,4,1 and 6 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 188416-27:
(8*1)+(7*8)+(6*8)+(5*4)+(4*1)+(3*6)+(2*2)+(1*7)=165
165 % 10 = 5
So 188416-27-5 is a valid CAS Registry Number.

188416-27-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name azane,2-chloro-6-ethyl-5-fluoro-1H-pyrimidin-4-one

1.2 Other means of identification

Product number -
Other names 2-chloro-6-ethyl-5-fluoro-1H-pyrimidin-4-one

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:188416-27-5 SDS

188416-27-5Relevant academic research and scientific papers

Preparation of triazoles by organometallic addition to ketones and intermediates therefor

-

, (2008/06/13)

A process for the preparation of a compound of the formula: or an acid addition or base salt thereof, wherein R is phenyl optionally substituted by 1 to 3 substituents each independently selected from halo and trifluoromethyl; R1 is C1-C6 alkyl; and “Het” is pyrimidinyl optionally substituted by 1 to 3 substituents each independently selected from C1-C4 alkyl, C1-C4 alkoxy, halo, oxo, benzyl and benzyloxy, comprising reacting a compound of the formula: with a compound of the formula wherein X is chloro, bromo or iodo, the reaction taking place in the presence of zinc; at least one of iodine or a Lewis acid; and an aprotic organic solvent: optionally further reacting the resulting compound with an acid or base to form the corresponding acid addition or base salt thereof.

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