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Benzamide, N-[2,2,2-trifluoro-1-(trifluoromethyl)ethyl]-, also known as 2,2,2-trifluoro-N-(trifluoromethyl)ethylbenzamide, is a chemical compound with the molecular formula C9H5F7NO. It is a derivative of benzamide, featuring a trifluoromethyl group and a trifluoroethyl group attached to the nitrogen atom. Benzamide, N-[2,2,2-trifluoro-1-(trifluoromethyl)ethyl]- is characterized by its fluorinated structure, which can contribute to unique chemical and physical properties, such as increased lipophilicity and stability. It is often used in the synthesis of pharmaceuticals and agrochemicals due to its potential to enhance the activity and selectivity of these compounds. The specific applications and properties of this benzamide derivative can vary widely depending on the context in which it is used, but its fluorinated nature is a key feature that sets it apart from other benzamide derivatives.

2151-49-7

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2151-49-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2151-49-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,5 and 1 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2151-49:
(6*2)+(5*1)+(4*5)+(3*1)+(2*4)+(1*9)=57
57 % 10 = 7
So 2151-49-7 is a valid CAS Registry Number.

2151-49-7SDS

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-(1,1,1,3,3,3-hexafluoropropan-2-yl)benzamide

1.2 Other means of identification

Product number -
Other names N-Benzoyl-hexafluorisopropylamin

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:2151-49-7 SDS

2151-49-7Relevant academic research and scientific papers

Interaction of bis(diisopropylamino)carbene with aroylimines activated by trifluoromethyl groups

Poliakov, Dmytro,Rogalyov, Alexey,Shevchenko, Igor

experimental part, p. 5805 - 5809 (2009/06/08)

Bis(diisopropylamino)carbene deoxygenates the carbonyl group of aroylimines Ar-C(O)-N=C(CF3)2 to form alkenes, which formally result from the coupling of two carbenes, [Ar-C(:)-N=C(CF3)2] and [(iPr2N)

Kinetic stability of novel nitrile ylides

Hegarty, Anthony F.,Eustace, Stephen J.,Tynan, Nuala M.,Pham-Tran, Nguyen-Nguyen,Nguyen, Minh Tho

, p. 1239 - 1246 (2007/10/03)

A series of relatively stable novel trifluoromethyl substituted nitrile ylides have been generated by base promoted elimination of hydrogen chloride from the corresponding imidoyl chlorides in acetonitrile and aqueous dioxane solution at 25 °C. The format

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