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3-fluoro-N-(3,4,5-trifluorobenzyl)aniline is a chemical compound characterized by the molecular formula C13H8F4N. It is a substituted aniline derivative, featuring a fluorine atom at the third carbon of the benzene ring and a trifluoromethyl group attached to the benzyl moiety. This unique structure endows the compound with specific properties, making it valuable in pharmaceutical and research applications. The presence of fluorine atoms in the molecule enhances its lipophilicity, potentially affecting its biological activity. However, due to its potential toxicity and reactivity, it requires careful handling in a controlled laboratory setting.

637744-49-1

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637744-49-1 Usage

Uses

Used in Pharmaceutical Applications:
3-fluoro-N-(3,4,5-trifluorobenzyl)aniline serves as a building block in the synthesis of various organic compounds, particularly those with pharmaceutical relevance. Its unique structure and enhanced lipophilicity contribute to the development of new drugs with improved bioavailability and efficacy.
Used in Research Applications:
In the field of research, 3-fluoro-N-(3,4,5-trifluorobenzyl)aniline is utilized as a reagent in chemical reactions, facilitating the synthesis of complex organic molecules. Its unique properties allow for the exploration of novel chemical pathways and the discovery of new compounds with potential applications in various industries.
Used in Chemical Reactions:
3-fluoro-N-(3,4,5-trifluorobenzyl)aniline is employed as a reagent in various chemical reactions, enabling the formation of new compounds with specific properties. Its fluorinated structure can influence the reaction outcomes, leading to the development of innovative materials and products.
Used in Controlled Laboratory Environments:
Due to its potential toxicity and reactive nature, 3-fluoro-N-(3,4,5-trifluorobenzyl)aniline is primarily used in controlled laboratory environments. Researchers and chemists handle the compound with caution, ensuring safety protocols are followed to minimize risks associated with its use.

Check Digit Verification of cas no

The CAS Registry Mumber 637744-49-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,3,7,7,4 and 4 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 637744-49:
(8*6)+(7*3)+(6*7)+(5*7)+(4*4)+(3*4)+(2*4)+(1*9)=191
191 % 10 = 1
So 637744-49-1 is a valid CAS Registry Number.

637744-49-1SDS

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 3-Fluoro-N-(3,4,5-trifluorobenzyl)aniline

1.2 Other means of identification

Product number -
Other names 3-fluoro-N-[(3,4,5-trifluorophenyl)methyl]aniline

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:637744-49-1 SDS

637744-49-1Relevant academic research and scientific papers

Discovery of novel quaternary ammonium derivatives of (3R)-quinuclidinyl carbamates as potent and long acting muscarinic antagonists

Prat, Maria,Buil, María Antonia,Fernández, Maria Dolors,Castro, Jordi,Monleón, Juan Manuel,Tort, Laia,Casals, Gaspar,Ferrer, Manuel,Huerta, Josep Maria,Espinosa, Snia,López, Manuel,Segarra, Victor,Gavald, Amadeu,Miralpeix, Montserrat,Ramos, Israel,Vilella, Dolors,González, Marisa,Córdoba, Mnica,Cárdenas, Alvaro,Antón, Francisca,Beleta, Jorge,Ryder, Hamish

, p. 3457 - 3461 (2011/06/24)

Novel quaternary ammonium derivatives of N,N-disubstituted (3R)-quinuclidinyl carbamates have been identified as potent M3 muscarinic antagonists with long duration of action in an in vivo model of bronchoconstriction. These compounds have also presented a high level of metabolic transformation (human liver microsomes). The synthesis, structure-activity relationships and biological evaluation of these compounds are reported.

Stable crystalline salt of (R)-3-fluorophenyl-3,4,5-trifluorobenzylcarbamic acid 1-azabiciyclo [2.2.2]oct-3-yl ester

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Page/Page column 7; 9-10, (2009/06/27)

The present invention refers to a stable crystalline salt of (R)-3-fluorophenyl- 3,4,5-trifluorobenzylcarbamic acid 1-azabicyclo [2.2.2]oct-3-yl ester of formula (I) and its use as medicament, in particular for the treatment of urinary incontinence or oth

NOVEL QUINUCLIDINE DERIVATIVES AND MEDICINAL COMPOSITIONS CONTAINING THE SAME

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Page 27, (2008/06/13)

Carbamates of formula (I) or pharmaceutically acceptable salts thereof, including quaternary ammonium salts of formula (II) are disclosed; as well as processes for their preparation, pharmaceutical compositions comprising them and their use in therapy as antagonists of M3 muscarinic receptors.

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