91225-68-2

Basic information

• Product Name: 2-(CHLOROMETHYL)-6-ETHYLTHIENO[2,3-D]PYRIMIDIN-4(3H)-ONE
• Synonyms: IFLAB-BB F2117-0117;2-(CHLOROMETHYL)-6-ETHYLTHIENO[2,3-D]PYRIMIDIN-4(3H)-ONE;2-CHLOROMETHYL-6-ETHYL-3H-THIENO[2,3-D]PYRIMIDIN-4-ONE
• CAS NO: 91225-68-2
• Molecular Formula: C9H9ClN2OS
• Molecular Weight: 228.7
• Mol File: 91225-68-2.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-(CHLOROMETHYL)-6-ETHYLTHIENO[2,3-D]PYRIMIDIN-4(3H)-ONE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(CHLOROMETHYL)-6-ETHYLTHIENO[2,3-D]PYRIMIDIN-4(3H)-ONE(91225-68-2)
• EPA Substance Registry System: 2-(CHLOROMETHYL)-6-ETHYLTHIENO[2,3-D]PYRIMIDIN-4(3H)-ONE(91225-68-2)

Safety Data

• Hazardous Substances Data: 91225-68-2(Hazardous Substances Data)

Usage

General Description

2-(Chloromethyl)-6-ethylthieno[2,3-d]pyrimidin-4(3H)-one is a chemical compound with potential pharmaceutical applications. It is a heterocyclic compound containing a thieno ring and a pyrimidine ring, as well as a chloromethyl and an ethyl group. The compound has been studied for its potential use in the development of pharmaceutical drugs, particularly in the treatment of various diseases and conditions. Its specific properties and potential uses in medicine make it an interesting compound for further research and development.

Upstream product

• 4507-13-5 ethyl 2-amino-5-ethylthiophene-3-carboxylate 
• 107-14-2 chloroacetonitrile 

Relevant articles and documents

Synthesis and antihyperlipidemic activity of some novel condensed 2-chloroalkyl-4-chloro/hydroxy-5,6-disubstituted pyrimidines

Synthesis and antihyperlipidemic activity of a series of novel condensed 2-chloroalkyl-4-chloro/hydroxy-5,6-di-substituted pyrimidines are described. The design of these compounds is based on the earlier QSAR study on the antihyperlipidemic 2-substituted

Reaction of Nitriles Under Acidic Conditions. Part III. A Facile Synthesis of Thienopyrimidin-4(3H)-ones

A variety of thiophene o-aminoesters were reacted with cyanates, thiocyanates, cyanamides, acyl cyanides and α-functionalized acetonitrile derivatives to yield the corresponding 2-substituted thienopyrimidin-4(3H)-ones.