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4-Chloro-2-phenylthieno[2,3-d]pyrimidine is a heterocyclic organic compound characterized by a thieno[2,3-d]pyrimidine core with a chloro group at the 4-position and a phenyl group at the 2-position. 4-chloro-2-phenylthieno[2,3-d]pyrimidine is known for its potential as a building block in organic synthesis and as a starting material for the preparation of pharmaceuticals, agrochemicals, and materials for electronic devices. Its unique structure and reactivity make it a valuable intermediate for the synthesis of diverse compounds, participating in various organic reactions such as nucleophilic substitution, cross-coupling, and cycloaddition reactions. 4-chloro-2-phenylthieno[2,3-d]pyrimidine has garnered interest among chemists and researchers for its potential utility in the development of new molecules with a wide range of applications.

56843-80-2

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56843-80-2 Usage

Uses

Used in Pharmaceutical Industry:
4-Chloro-2-phenylthieno[2,3-d]pyrimidine is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique structure and reactivity allow for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical industry, 4-chloro-2-phenylthieno[2,3-d]pyrimidine serves as a starting material for the preparation of agrochemicals, such as pesticides and herbicides. Its ability to participate in various organic reactions enables the synthesis of novel agrochemicals with improved efficacy and selectivity.
Used in Electronic Materials Industry:
4-Chloro-2-phenylthieno[2,3-d]pyrimidine is utilized as a building block for the development of materials for electronic devices, such as organic semiconductors and optoelectronic materials. Its unique electronic properties and compatibility with various synthetic routes make it a promising candidate for the creation of advanced electronic materials.
Used in Organic Synthesis:
As a versatile intermediate in organic synthesis, 4-chloro-2-phenylthieno[2,3-d]pyrimidine is employed in the preparation of a wide range of organic compounds. Its ability to undergo nucleophilic substitution, cross-coupling, and cycloaddition reactions allows for the synthesis of diverse molecules with potential applications in various fields, including pharmaceuticals, agrochemicals, and materials science.

Check Digit Verification of cas no

The CAS Registry Mumber 56843-80-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,8,4 and 3 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 56843-80:
(7*5)+(6*6)+(5*8)+(4*4)+(3*3)+(2*8)+(1*0)=152
152 % 10 = 2
So 56843-80-2 is a valid CAS Registry Number.
InChI:InChI=1/C12H7ClN2S/c13-10-9-6-7-16-12(9)15-11(14-10)8-4-2-1-3-5-8/h1-7H

56843-80-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Chloro-2-phenylthieno[2,3-d]pyrimidine

1.2 Other means of identification

Product number -
Other names 4-chloro-2-phenylthieno[2,3-d]pyrimidine

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:56843-80-2 SDS

56843-80-2Relevant academic research and scientific papers

Direct metallation of thienopyrimidines using a mixed lithium-cadmium base and antitumor activity of functionalized derivatives

Snegaroff, Katia,Lassagne, Frederic,Bentabed-Ababsa, Ghenia,Nassar, Ekhlass,Ely, Sidaty Cheikh Sid,Stephanie Hesse,Perspicace, Enrico,Derdour, Aicha,Mongin, Florence

experimental part, p. 4782 - 4788 (2009/12/08)

A series of thieno[2,3-d]- and thieno[3,2-d]pyrimidines have been easily synthesized using as key step a deproto-cadmiation-trapping sequence. Some of the compounds thus synthesized were screened for anticancer (cytotoxic) activities, and (S)-2-(6-iodo-2-

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