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4,6-Dichloro-2-(4-fluoro-phenyl)quinazoline is an organic compound that features a quinazoline core, a fundamental structure prevalent in numerous pharmaceutical drugs, with two chlorine atoms and a fluorophenyl group. As a quinazoline derivative, it is frequently utilized in medicinal chemistry research, where it acts as a precursor to more complex compounds through a variety of chemical reactions. The incorporation of both chlorine and fluorine atoms in its structure provides a wide range of opportunities for further substitutions, rendering it adaptable for the synthesis of diverse quinazoline derivatives. It is significant due to its potential involvement in drug synthesis. 4,6-DICHLORO-2-(4-FLUORO-PHENYL)-QUINAZOLINE is typically synthesized in a laboratory under controlled conditions and is not found naturally. The safety measures and potential risks associated with this chemical are similar to those of related chemicals, necessitating careful handling.

461036-88-4

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461036-88-4 Usage

Uses

Used in Medicinal Chemistry Research:
4,6-Dichloro-2-(4-fluoro-phenyl)quinazoline is used as a chemical precursor for the synthesis of more complex compounds in medicinal chemistry. Its presence as a quinazoline derivative allows for the development of new pharmaceutical drugs with potential therapeutic applications.
Used in Drug Synthesis:
4,6-DICHLORO-2-(4-FLUORO-PHENYL)-QUINAZOLINE is employed as a key intermediate in the synthesis of various drugs, particularly those that require the quinazoline core structure. The presence of chlorine and fluorine atoms on its structure facilitates further chemical reactions, making it a versatile building block for drug development.
Used in Laboratory Settings:
4,6-Dichloro-2-(4-fluoro-phenyl)quinazoline is used as a research compound in controlled laboratory environments. Its synthesis and subsequent reactions are studied to understand its potential applications and to develop new methodologies for the creation of pharmaceutical compounds.
Used in Chemical Synthesis Education:
In educational settings, particularly in chemistry courses, 4,6-dichlor0-2-(4-fluoro-phenyl)quinazoline can be used as a teaching aid to demonstrate the principles of organic synthesis, substitution reactions, and the role of functional groups in drug design.

Check Digit Verification of cas no

The CAS Registry Mumber 461036-88-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,6,1,0,3 and 6 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 461036-88:
(8*4)+(7*6)+(6*1)+(5*0)+(4*3)+(3*6)+(2*8)+(1*8)=134
134 % 10 = 4
So 461036-88-4 is a valid CAS Registry Number.
InChI:InChI=1S/C15H10Cl2N2O/c1-20-11-5-2-9(3-6-11)15-18-13-7-4-10(16)8-12(13)14(17)19-15/h2-8H,1H3

461036-88-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,6-dichloro-2-(4-fluorophenyl)quinazoline

1.2 Other means of identification

Product number -
Other names 4,6-DICHLORO-2-(4-FLUORO-PHENYL)-QUINAZOLINE

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:461036-88-4 SDS

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