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Benzene, 1-bromo-4-(2-chloro-1,1,2-trifluoroethoxy)-, also known as 1-bromo-4-(2-chloro-1,1,2-trifluoroethoxy)benzene, is an organic compound with the molecular formula C8H5BrClF3O. It is a halogenated derivative of benzene, featuring a bromine atom at the 1-position, a chlorine atom at the 2-position of the ethoxy group, and three fluorine atoms attached to the carbon atom in the ethoxy group. Benzene, 1-bromo-4-(2-chloro-1,1,2-trifluoroethoxy)- is characterized by its unique structure, which combines the properties of benzene with the reactivity of halogens and the electronegativity of fluorine. It is used in various chemical reactions and synthesis processes, particularly in the production of pharmaceuticals and agrochemicals, due to its ability to act as a precursor or intermediate in the formation of more complex molecules.

403-60-1

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403-60-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 403-60-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,0 and 3 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 403-60:
(5*4)+(4*0)+(3*3)+(2*6)+(1*0)=41
41 % 10 = 1
So 403-60-1 is a valid CAS Registry Number.

403-60-1Relevant academic research and scientific papers

Base-catalyzed stereoselective hydrophenoxylation and hydrothiolation of hexafluorobutyne

Bo, Zhao,Dong-Huai, Tu,Ji-Jun, Zeng,Jian, Lu,Jiang-Wei, Li,Sheng, Han,Wei, Zhang

, (2020)

Novel base-catalyzed hydrophenoxylation and hydrothiolation of hexafluorobutyne are described. By using an easily available base, a variety of vinyl ethers as well as sulfides are prepared at room temperature through two-phase nucleophilic addition reacti

Phenols reactions with 1,1-difluorodichloroethene, 1,2-di(fluorochloro) ethene, and trifluorochloroethene

Kremlev,Mushta,Moklyarchuk

, p. 1125 - 1129 (2007/10/03)

Phenols containing in the para-position of the benzene ring substituents of various electronic character add to 1,1-difluorodichloroethene in acetone in the presence of potassium hydroxide. A similar reaction with 1,2-di(fluorochloro)ethene occurs only in

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