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N,N-diethyl-2-oxo-2-{[3-(trifluoromethyl)phenyl]amino}ethanaminium is a complex organic compound with the molecular formula C14H18F3N2O. It is a cationic species, which means it carries a positive charge. The compound features a central ethanaminium (ethylated amine) structure with a carbonyl group (C=O) at the 2-position, indicating the presence of an amide or ester functionality. The amino group is attached to a phenyl ring, which is substituted with a trifluoromethyl group at the 3-position. This trifluoromethyl group imparts unique electronic and steric properties to the molecule. The two ethyl groups attached to the nitrogen atom contribute to the overall lipophilicity and may influence the compound's solubility and reactivity. This chemical structure suggests potential applications in various fields, such as pharmaceuticals, agrochemicals, or materials science, where its specific properties could be exploited for specific functions or reactions.

6833-52-9

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6833-52-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6833-52-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,8,3 and 3 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6833-52:
(6*6)+(5*8)+(4*3)+(3*3)+(2*5)+(1*2)=109
109 % 10 = 9
So 6833-52-9 is a valid CAS Registry Number.

6833-52-9SDS

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 diethyl-[2-oxo-2-[3-(trifluoromethyl)anilino]ethyl]azanium

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:6833-52-9 SDS

6833-52-9Relevant academic research and scientific papers

Access to Optically Enriched α-Aryloxycarboxylic Esters via Carbene-Catalyzed Dynamic Kinetic Resolution and Transesterification

Liu, Bin,Song, Runjiang,Xu, Jun,Majhi, Pankaj Kumar,Yang, Xing,Yang, Song,Jin, Zhichao,Chi, Yonggui Robin

supporting information, p. 3335 - 3338 (2020/04/30)

Optically active α-aryloxycarboxylic acids and their derivatives are important functional molecules. Disclosed here is a carbene-catalyzed dynamic kinetic resolution and transesterification reaction for access to this class of molecules with up to 99% yields and 99:1 er values. Addition of a chiral carbene catalyst to the ester substrate leads to two diastereomeric azolium ester intermediates that can quickly epimerize to each other and thus allows for effective dynamic kinetic resolution to be realized. The optically enriched ester products from our reaction can be quickly transformed to chiral herbicides and other bioactive molecules.

Copper-catalyzed one-pot synthesis of 2H-1,4-benzoxazin-3-(4H)-ones from 2-(o-haloaryloxy)acyl chlorides and primary amines

Hu, Qunxian,Xia, Ziming,Fan, Ling,Zheng, Jiening,Wang, Xiaoxia,Lv, Xin

experimental part, p. 129 - 142 (2012/05/04)

A facile and efficient Cu(I)-catalyzed one-pot synthesis of 2H-1,4-benzoxazin-3-(4H)-one derivatives has been developed. The condensation between 2-(o-haloaryloxy)acyl chlorides and primary amines followed by Cu(I)-catalyzed intramolecular C-N bond coupling afforded a variety of 2H-1,4-benzoxazin-3-(4H)-ones in good to excellent yields. Diversified substitutents on the 4-position could be conveniently introduced. ARKAT-USA, Inc.

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