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25771-21-5

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25771-21-5 Usage

General Description

N,N-dimethyl-4-(trifluoromethyl)benzamide is a chemical compound with the molecular formula C10H10F3NO. It is a derivative of benzamide, with a trifluoromethyl group attached to the fourth position of the benzene ring and two methyl groups attached to the nitrogen atom. N,N-dimethyl-4-(trifluoromethyl)benzamide is commonly used as an intermediate in organic synthesis and pharmaceutical research. Its unique structure and properties make it a valuable building block for the creation of various drugs and bioactive compounds. Furthermore, the trifluoromethyl group is known for its ability to enhance the biological activity and metabolic stability of pharmaceutical compounds, making N,N-dimethyl-4-(trifluoromethyl)benzamide a versatile and important chemical in medicinal chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 25771-21-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,7,7 and 1 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 25771-21:
(7*2)+(6*5)+(5*7)+(4*7)+(3*1)+(2*2)+(1*1)=115
115 % 10 = 5
So 25771-21-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H10F3NO/c1-14(2)9(15)7-3-5-8(6-4-7)10(11,12)13/h3-6H,1-2H3

25771-21-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N-Dimethyl-4-(trifluoromethyl)benzamide

1.2 Other means of identification

Product number -
Other names 4-trifluoromethylbenzoic acid N,N-dimethylamide

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:25771-21-5 SDS

25771-21-5Relevant articles and documents

Azulene-based compounds for targeting orexin receptors

Leino, Teppo O.,Turku, Ainoleena,Yli-Kauhaluoma, Jari,Kukkonen, Jyrki P.,Xhaard, Henri,Wallén, Erik A.A.

, p. 88 - 100 (2018)

A library of 70 000 synthetically accessible azulene-based compounds was virtually screened at the OX2 receptor. Based on the results, a series of azulene derivatives was synthesized and the binding to and activation of both orexin receptor subtypes were assessed. Two most promising binders were determined to have inhibition constants in the 3–9 μM range and two other compounds showed weak OX2 receptor agonism. Furthermore, three compounds exhibited a concentration-dependent potentiation of the response to orexin-A at the OX1 but not the OX2 receptors. Altogether this data opens new approaches for further development of antagonists, agonists, and potentiators of orexin response based on the azulene scaffold.

Rhoda-Electrocatalyzed Bimetallic C?H Oxygenation by Weak O-Coordination

Tan, Xuefeng,Massignan, Leonardo,Hou, Xiaoyan,Frey, Johanna,Oliveira, Jo?o C. A.,Hussain, Masoom Nasiha,Ackermann, Lutz

supporting information, p. 13264 - 13270 (2021/05/06)

Rhodium-electrocatalyzed arene C?H oxygenation by weakly O-coordinating amides and ketones have been established by bimetallic electrocatalysis. Likewise, diverse dihydrooxazinones were selectively accessed by the judicious choice of current, enabling twofold C?H functionalization. Detailed mechanistic studies by experiment, mass spectroscopy and cyclovoltammetric analysis provided support for an unprecedented electrooxidation-induced C?H activation by a bimetallic rhodium catalysis manifold.

A scalable continuous photochemical process for the generation of aminopropylsulfones

Baumann, Marcus,Bonciolini, Stefano,Di Filippo, Mara

supporting information, p. 9428 - 9432 (2020/12/15)

An efficient continuous photochemical process is presented that delivers a series of novel γ-aminopropylsulfones via a tetrabutylammonium decatungstate (TBADT) catalysed HAT-process. Crucial to this success is the exploitation of a new high-power LED emitting at 365 nm that was found to be superior to an alternative medium-pressure Hg lamp. The resulting flow process enabled the scale-up of this transformation reaching throughputs of 20 mmol h-1 at substrate concentrations up to 500 mM. Additionally, the substrate scope of this transformation was evaluated demonstrating the straightforward incorporation of different amine substituents as well as alkyl appendages next to the sulfone moiety. It is anticipated that this methodology will allow for further exploitations of these underrepresented γ-aminopropylsulfone scaffolds in the future. This journal is

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