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3574-96-7

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3574-96-7 Usage

Description

Chlorfenazole, also known as 2-(2-Chlorophenyl)-1H-benzimidazole, is a benzimidazole derivative with anti-parasitic, anti-fungal, and anti-inflammatory properties. It is a biologically active compound that has been used as an agricultural chemical.

Uses

Used in Agricultural Chemicals:
Chlorfenazole is used as an agricultural chemical to control pests and diseases in crops. Its anti-parasitic and anti-fungal properties make it effective in protecting plants from various threats.
Used in Anti-parasitic Applications:
Chlorfenazole is used as an anti-parasitic agent to treat infections caused by parasites. Its ability to target and eliminate parasites makes it a valuable tool in combating parasitic diseases.
Used in Anti-fungal Applications:
Chlorfenazole is used as an anti-fungal agent to treat fungal infections. Its anti-fungal properties help in controlling the growth and spread of fungi, thereby preventing fungal diseases.
Used in Anti-inflammatory Applications:
Chlorfenazole is used as an anti-inflammatory agent to reduce inflammation and alleviate pain. Its anti-inflammatory properties make it useful in treating conditions characterized by inflammation.

Hazard

A poison by ingestion.

Safety Profile

A poison by ingestion. When heated to decomposition it emits toxic vapors of NOx and Cl-.

Check Digit Verification of cas no

The CAS Registry Mumber 3574-96-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,7 and 4 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3574-96:
(6*3)+(5*5)+(4*7)+(3*4)+(2*9)+(1*6)=107
107 % 10 = 7
So 3574-96-7 is a valid CAS Registry Number.
InChI:InChI=1/C13H9ClN2/c14-10-6-2-1-5-9(10)13-15-11-7-3-4-8-12(11)16-13/h1-8H,(H,15,16)

3574-96-7 Well-known Company Product Price

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  • (Code)Product description
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  • Alfa Aesar

  • (L07631)  2-(2-Chlorophenyl)benzimidazole, 98%   

  • 3574-96-7

  • 5g

  • 545.0CNY

  • Detail
  • Alfa Aesar

  • (L07631)  2-(2-Chlorophenyl)benzimidazole, 98%   

  • 3574-96-7

  • 25g

  • 2189.0CNY

  • Detail
  • Aldrich

  • (632600)  2-(2-Chlorophenyl)benzimidazole  97%

  • 3574-96-7

  • 632600-5G

  • 423.54CNY

  • Detail
  • Aldrich

  • (632600)  2-(2-Chlorophenyl)benzimidazole  97%

  • 3574-96-7

  • 632600-25G

  • 1,883.70CNY

  • Detail

3574-96-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name chlorfenazole

1.2 Other means of identification

Product number -
Other names 2-(2-Chlorophenyl)benzimidazole

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:3574-96-7 SDS

3574-96-7Relevant articles and documents

A new facile synthesis of 11-oxo-10,11-dihydro-5H-dibenzo[b,e][1,4]diazepines

Giani,Borsa,Parini,Tonon

, p. 550 - 552 (1985)

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[Diaquo{bis(p-hydroxybenzoato-κ1O1)}(1-methylimidazole- κ1N1)}copper(II)]: Synthesis, crystal structure, catalytic activity and DFT study

Brahman, Dhiraj,Chhetri, Sailesh,Kamath, Amarjit,McArdle, Patrick,Sinha, Biswajit

, (2021/09/04)

Metal-organic hybrid complexes often exhibit large surface area, pore volume, fascinating structures and potential applications including catalytic applications. Hence a new metal-organic hybrid complex [Diaquo{bis(p-hydroxybenzoato-κ1O1)}(1-methylimidazole- κ1N1)}copper(II)] was synthesized using conventional method. Physico-chemical characterization of the complex was performed with FTIR spectroscopy, single crystal X-ray diffraction, TGA, EPR and FESEM. Single crystal X-ray diffraction study suggests it to be three dimensional with space group P212121 (orthorhombic). The crystal achieves its three-dimensional structure and stability through extensive intermolecular hydrogen bonding. Hirshfeld surface analysis, catalytic activity and DFT study of the complex was also performed. The synthesized complex acts as good catalyst in benzimidazole synthesis with good recyclability as catalyst up to 5th run.

1-Methylimidazolium ionic liquid supported on Ni@zeolite-Y: fabrication and performance as a novel multi-functional nanocatalyst for one-pot synthesis of 2-aminothiazoles and 2-aryl benzimidazoles

Kalhor, Mehdi,Zarnegar, Zohre

, p. 519 - 540 (2021/12/03)

In the present study, 1-methyl-3-(3-trimethoxysilylpropyl)-1H-imidazol-3-ium chloride-supported Ni@zeolite-Y-based nanoporous materials (Ni@zeolite-Im-IL) were synthesized and their structures were confirmed using different characterization techniques such as FT-IR, FE-SEM, EDX, XRD, BET and TGA-DTG analyses. In order to synthesize this multi-functional nano-system, zeolite-NaY was modified first, with exchanged Ni2+ ions and 3-chloropropyltriethoxysilane (CPTES) as a coupling reagent and then functionalized to imidazolium chloride ionic liquid by N-methylimidazole. New multi-functional nano-material of Ni@zeolite-Im-IL demonstrated high activity in the catalytic synthesis of 2-aminothiazoles 3a–l by one-pot reaction of methylcarbonyls, thiourea and iodine at 80?°C in DMSO with good to excellent yields (85–98%). Also, the catalytic synthesis of 2-aryl benzimidazoles, 6a–m was performed by the condensational reaction of o-arylendiamine and aromatic aldehydes in EtOH at room temperature with excellent yields (90–98%). Advantages of this efficient synthetic strategy include higher purity and shorter reaction time, excellent yield, easy isolation of products, the good stability, activity and feasible reusability of the metallic ionic liquid nanocatalyst. These benefits have made this method more compatible with the principles of green chemistry. Graphical abstract: [Figure not available: see fulltext.]

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