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2-(dimethylamino)-5-(trifluoromethyl)benzaldehyde is an aromatic compound characterized by a molecular formula of C10H10F3NO. It features a benzene ring with a dimethylamino group and a trifluoromethyl group, complemented by an aldehyde functional group. 2-(dimethylamino)-5-(trifluoromethyl)benzaldehyde is notable for its role in the synthesis of various products and its applications in different fields due to the unique properties conferred by its substituents.

945847-58-5

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945847-58-5 Usage

Uses

Used in Pharmaceutical Industry:
2-(dimethylamino)-5-(trifluoromethyl)benzaldehyde serves as an intermediate in the synthesis of pharmaceuticals, where its presence can modulate the pharmacokinetic and pharmacodynamic properties of the resulting molecules. The dimethylamino and trifluoromethyl groups are particularly important in medicinal chemistry for their ability to influence the potency, selectivity, and metabolic stability of drug candidates.
Used in Agrochemical Industry:
In the agrochemical sector, 2-(dimethylamino)-5-(trifluoromethyl)benzaldehyde is utilized as a precursor in the production of various agrochemicals. Its unique structural features contribute to the development of compounds with specific pesticidal or herbicidal activities, enhancing crop protection strategies.
Used in Dye Industry:
2-(dimethylamino)-5-(trifluoromethyl)benzaldehyde is also employed in the dye industry, where it contributes to the creation of dyes with particular color characteristics and properties. Its chemical structure allows for the development of dyes that may have specific applications in textiles, printing, or other industries requiring colorants.
Used in Organic Chemistry as a Reagent:
2-(dimethylamino)-5-(trifluoromethyl)benzaldehyde functions as a reagent in organic chemistry, particularly in reactions involving the formation of carbon-carbon and carbon-heteroatom bonds. Its presence can facilitate complex organic synthesis, leading to the production of a wide range of organic compounds for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 945847-58-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,5,8,4 and 7 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 945847-58:
(8*9)+(7*4)+(6*5)+(5*8)+(4*4)+(3*7)+(2*5)+(1*8)=225
225 % 10 = 5
So 945847-58-5 is a valid CAS Registry Number.

945847-58-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name Benzaldehyde, 2-(dimethylamino)-5-(trifluoromethyl)-

1.2 Other means of identification

Product number -
Other names 2-Dimethylamino-5-trifluoromethylbenzaldehyde

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:945847-58-5 SDS

945847-58-5Downstream Products

945847-58-5Relevant academic research and scientific papers

TRISUBSTITUTED AMINE COMPOUNDS AS INHIBITORS OF -CHOLESTERYL ESTER TRANSFER PROTEIN CETP

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Page/Page column 102, (2008/06/13)

The present invention relates to a compound of the general formula (1): (1)wherein, Y is a methylene group, and the like; A is an optionally substituted heterocyclic group, and the like; B is an optionally substituted phenyl group, and the like; R1 is an optionally substituted alkyl group, and the like; and R2 is an optionally substituted amino group, and the like; or a pharmaceutically acceptable derivative thereof, which has an inhibitory activity against cholesteryl ester transfer protein (CETP), thereby being useful for prophylaxis and/or treatment of arteriosclerotic diseases, hyperlipemia or dyslipidemia, and the like.

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