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1H-1,2,4-Triazole, 1-[2-(bromomethyl)-4-chlorophenyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

404922-80-1

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404922-80-1 Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 9 carbon (C), 7 hydrogen (H), 1 bromine (Br), 1 chlorine (Cl), and 3 nitrogen (N) atoms.

Explanation

The compound is a derivative of 1H-1,2,4-triazole, which is a five-membered heterocyclic ring containing three nitrogen atoms and two carbon atoms. It has a substituted phenyl ring (a six-membered carbon ring with alternating single and double bonds) attached to it.

Explanation

The compound contains a bromomethyl (-CH2Br) group and a chlorophenyl (-C6H4Cl) group, which are attached to the phenyl ring. These substituents can influence the compound's reactivity and biological activity.

Explanation

Triazoles, in general, have a wide range of pharmacological activities, such as antifungal, antibacterial, and anticancer properties. This specific compound, due to its unique structure and substituents, may have potential applications in the development of new drugs.

Explanation

The compound's triazole core and its substituents may contribute to its potential pharmacological activities, which include fighting fungal infections, bacterial infections, and cancer cells.

Explanation

Due to its unique structure and potential pharmacological activities, 1H-1,2,4-Triazole, 1-[2-(bromomethyl)-4-chlorophenyl]is an important target for further research and development in the field of pharmaceutical chemistry. This may lead to the discovery of new drugs with improved efficacy and safety profiles.

Chemical structure

1H-1,2,4-Triazole derivative with a substituted phenyl ring

Substituents

Bromomethyl and chlorophenyl groups

Potential applications

Medicinal chemistry and drug development

Pharmacological activities

Antifungal, antibacterial, and anticancer properties

Importance in pharmaceutical chemistry

Target for further research and development

Check Digit Verification of cas no

The CAS Registry Mumber 404922-80-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,4,9,2 and 2 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 404922-80:
(8*4)+(7*0)+(6*4)+(5*9)+(4*2)+(3*2)+(2*8)+(1*0)=131
131 % 10 = 1
So 404922-80-1 is a valid CAS Registry Number.

404922-80-1SDS

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 1-[2-(bromomethyl)-4-chlorophenyl]-1,2,4-triazole

1.2 Other means of identification

Product number -
Other names 1H-1,2,4-Triazole,1-[2-(bromomethyl)-4-chlorophenyl]

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:404922-80-1 SDS

404922-80-1Relevant academic research and scientific papers

Development of an oxazolopyridine series of dual thrombin/factor Xa inhibitors via structure-guided lead optimization

Deng, James Z.,McMasters, Daniel R.,Rabbat, Philippe M.A.,Williams, Peter D.,Coburn, Craig A.,Yan, Youwei,Kuo, Lawrence C.,Lewis, S. Dale,Lucas, Bobby J.,Krueger, Julie A.,Strulovici, Berta,Vacca, Joseph P.,Lyle, Terry A.,Burgey, Christopher S.

, p. 4411 - 4416 (2007/10/03)

Thrombin-inhibitor X-ray crystal structures, in combination with the installation of binding elements optimized within the pyrazinone series of thrombin inhibitors, were utilized to transform a weak triazolopyrimidine lead into a series of potent oxazolop

Thrombin inhibitors

-

Page 21, (2008/06/13)

Compounds of the invention are useful in inhibiting thrombin and associated thrombotic occlusions having the following structure: or a pharmaceutically acceptable salt thereof.

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