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N-[3-(TrifluoroMethyl)phenyl]benzenesulfonaMide, 97%, is a high-purity chemical compound with the molecular formula C14H10F3NO2S. It is characterized by the presence of a trifluoromethyl group attached to a phenyl ring, which is connected to another phenyl ring through a sulfonamide linkage. N-[3-(TrifluoroMethyl)phenyl]benzenesulfonaMide, 97% is known for its potential applications in the synthesis of pharmaceuticals and agrochemicals, where it may serve as an intermediate or a building block for more complex molecules. The 97% purity indicates that the product is of high quality, with minimal impurities, which is crucial for its use in sensitive chemical reactions and to ensure the safety and efficacy of the final products.

2805-88-1

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2805-88-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2805-88-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,0 and 5 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2805-88:
(6*2)+(5*8)+(4*0)+(3*5)+(2*8)+(1*8)=91
91 % 10 = 1
So 2805-88-1 is a valid CAS Registry Number.
InChI:InChI=1/C13H10F3NO2S/c14-13(15,16)10-5-4-6-11(9-10)17-20(18,19)12-7-2-1-3-8-12/h1-9,17H

2805-88-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[3-(trifluoromethyl)phenyl]benzenesulfonamide

1.2 Other means of identification

Product number -
Other names HMS1536A16

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:2805-88-1 SDS

2805-88-1Relevant academic research and scientific papers

Copper-catalyzed N-arylation of sulfonamides with boronic acids in water under ligand-free and aerobic conditions

Nasrollahzadeh, Mahmoud,Ehsani, Ali,Maham, Mehdi

, p. 505 - 508 (2014/03/21)

An efficient and novel method for the copper-catalyzed arylation of sulfonamides in water under ligand-free conditions is reported. The significant advantages of this methodology are high yields, simple workup procedure, and elimination of toxic materials

Nanocopper-mediated direct arylsulfonamidation of aryl halides with arylsulfonyl azides

Yavari,Solgi,Ghazanfarpour-Darjani,Ahmadian

, p. 977 - 981 (2013/02/23)

An efficient protocol for direct arylsulfonamidation of aryl iodides and aryl bromides using arylsulfonylazides catalyzed by copper nanoparticles is described. Iranian Chemical Society 2012.

Copper-catalysed N-arylation of arylsulfonamides with aryl bromides and aryl iodides using KF/Al2O3

Hosseinzadeh, Rahman,Tajbakhsh, Mahmood,Mohadjerani, Maryam,Alikarami, Mohammad

experimental part, p. 143 - 148 (2010/11/16)

An efficient synthesis of N-arylsulfonamides with a variety of aryl bromides, aryl iodides and heteroaryl bromides using KF/Al2O 3 as a suitable base, CuI as an inexpensive catalyst and N,N′dimethylethylenediamine (N,N′-DMEDA) as an effective ligand is described. Indian Academy of Sciences.

SULFAMOYL BENZOIC ACID DERIVATIVES AS TRPM8 ANTAGONISTS

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Page/Page column 43, (2010/11/17)

The present invention relates to sulfamoyl benzoic acid derivatives of formula (I) or a pharmaceutically acceptable salt thereof, processes for their preparation, pharmaceutical compositions containing them and their use in the treatment of various disorders which are mediated via the TRPM8 receptor.

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