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870450-89-8

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870450-89-8 Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 15 carbon (C) atoms, 10 hydrogen (H) atoms, 6 fluorine (F) atoms, and 2 nitrogen (N) atoms.

Explanation

The compound is derived from benzimidazole, which is a fused ring system consisting of a benzene ring and an imidazole ring. The phenyl group (a six-carbon ring) is attached to the benzimidazole, and it has two trifluoromethyl groups (-CF3) attached at the 3rd and 5th positions.

Explanation

The compound is used as a building block for the synthesis of various pharmaceuticals due to its unique chemical structure and properties.

Explanation

The compound has shown potential in exhibiting anti-cancer and anti-inflammatory effects, making it a valuable candidate for further research and development in the field of medicine.

Explanation

The unique chemical structure and properties of the compound make it useful for studying various chemical reactions and biological processes, contributing to a better understanding of these phenomena.

Explanation

The presence of six fluorine atoms in the molecular structure contributes to the compound's unique properties, such as increased lipophilicity and potential for hydrogen bonding, which can be beneficial in drug development.

Explanation

The compound's stability allows it to be used in various chemical reactions and biological assays without undergoing significant degradation or decomposition.

Chemical structure

Benzimidazole derivative with a phenyl group substituted with two trifluoromethyl groups at the 3 and 5 positions.

Application

Medicinal chemistry and drug development.

Biological activity

Anti-cancer and anti-inflammatory properties.

Research utility

Valuable tool in the study of chemical reactions and biological processes.

Fluorine content

Contains six fluorine atoms.

Stability

Relatively stable under various conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 870450-89-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,0,4,5 and 0 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 870450-89:
(8*8)+(7*7)+(6*0)+(5*4)+(4*5)+(3*0)+(2*8)+(1*9)=178
178 % 10 = 8
So 870450-89-8 is a valid CAS Registry Number.
InChI:InChI=1/C15H8F6N2/c16-14(17,18)9-5-10(15(19,20)21)7-11(6-9)23-8-22-12-3-1-2-4-13(12)23/h1-8H

870450-89-8SDS

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 1-[3,5-bis(trifluoromethyl)phenyl]benzimidazole

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:870450-89-8 SDS

870450-89-8Downstream Products

870450-89-8Relevant articles and documents

A soluble base for the copper-catalyzed imidazole N-arylations with aryl halides

Liu, Longbin,Frohn, Mike,Xi, Ning,Dominguez, Celia,Hungate, Randy,Reider, Paul J.

, p. 10135 - 10138 (2005)

CuI-catalyzed N-arylation of imidazoles with aryl bromides has been achieved in a near-homogeneous system that utilizes tetraethylammonium carbonate as base, 8-hydroxyquinoline as ligand, and H2O as cosolvent. Preliminary results with aryl chlo

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