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2-(Chloromethyl)-6-ethylthieno[2,3-d]pyrimidin-4(3H)-one is a heterocyclic chemical compound that features a thieno ring and a pyrimidine ring, along with a chloromethyl and an ethyl group. 2-(CHLOROMETHYL)-6-ETHYLTHIENO[2,3-D]PYRIMIDIN-4(3H)-ONE is of interest in the pharmaceutical industry due to its potential applications in the development of drugs for the treatment of various diseases and conditions.

91225-68-2

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91225-68-2 Usage

Uses

Used in Pharmaceutical Industry:
2-(Chloromethyl)-6-ethylthieno[2,3-d]pyrimidin-4(3H)-one is used as a potential pharmaceutical compound for its potential role in the development of new drugs. 2-(CHLOROMETHYL)-6-ETHYLTHIENO[2,3-D]PYRIMIDIN-4(3H)-ONE's unique structure and properties make it a candidate for further research and development in medicine.
Used in Drug Development:
2-(Chloromethyl)-6-ethylthieno[2,3-d]pyrimidin-4(3H)-one is used as a chemical intermediate in the synthesis of pharmaceutical drugs. Its presence in the molecular structure can contribute to the drug's efficacy and therapeutic potential, making it a valuable component in the creation of new medications.
Used in Research and Development:
2-(Chloromethyl)-6-ethylthieno[2,3-d]pyrimidin-4(3H)-one is used as a research compound in the study of its chemical properties and potential interactions with biological systems. This research can lead to a better understanding of the compound's role in medicine and its potential applications in the treatment of various diseases and conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 91225-68-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,2,2 and 5 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 91225-68:
(7*9)+(6*1)+(5*2)+(4*2)+(3*5)+(2*6)+(1*8)=122
122 % 10 = 2
So 91225-68-2 is a valid CAS Registry Number.

91225-68-2SDS

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-(chloromethyl)-6-ethyl-3H-thieno[2,3-d]pyrimidin-4-one

1.2 Other means of identification

Product number -
Other names -

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:91225-68-2 SDS

91225-68-2Downstream Products

91225-68-2Relevant academic research and scientific papers

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

Kathiravan, Matthu K.,Shishoo, Chamanlal J.,Kumar, Krishnan Girish,Roy, Saroj Kumar,Mahadik, Kakasheb R.,Kadam, Shivajirao S.,Jain, Kishor S.

, p. 599 - 606 (2008/03/13)

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

Synthesis and pharmacological study of antihyperlipaemic activity of 2-substituted thieno(2,3-d)pyrimidin-4(3H)-ones

Shishoo,Devani,Bhadti,Jain,Rathod,Goyal,Gandhi,Patel,Naik

, p. 567 - 572 (2007/10/02)

A series of 2-substituted thieno(2,3-d)pyrimidin-4-(3H)-ones (1-15) was prepared by the reaction of thiophene ortho-aminoester (IV) with a variety of nitriles (V) under acidic conditions, and screened for antihyperlipaemic activity in various and animals

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

Shishoo, C. J.,Devani, M. B.,Pathak, U. S.,Ananthan, S.,Bhadti, V. S.,et al.

, p. 375 - 380 (2007/10/02)

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.

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