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1-bromo-2-fluoro-4-(2,2,2-trifluoroethoxy)benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1036724-63-6

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1036724-63-6 Usage

Chemical structure

A benzene ring with bromine, fluorine, and a trifluoroethoxy group attached to it.

Classification

Halogenated aromatic compound.

Functional groups

Bromine, fluorine, and trifluoroethoxy (ether) group.

Applications

a. Organic synthesis.
b. Building block for pharmaceuticals and agrochemicals.
c. Material science for the development of new materials with specific properties.

Reactivity

Unique reactivity and interactions with other substances due to the presence of multiple halogen atoms.

Importance

An important target for research and development in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 1036724-63-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,6,7,2 and 4 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1036724-63:
(9*1)+(8*0)+(7*3)+(6*6)+(5*7)+(4*2)+(3*4)+(2*6)+(1*3)=136
136 % 10 = 6
So 1036724-63-6 is a valid CAS Registry Number.

1036724-63-6Downstream Products

1036724-63-6Relevant academic research and scientific papers

HETEROCYCLIC COMPOUNDS AS DELTA-5 DESATURASE INHIBITORS AND METHODS OF USE

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Page/Page column 100-101, (2021/06/04)

The present disclosure provides compounds useful for the inhibition of Delta-5 Desaturase ("D5D"). The compounds have a general Formula (I): wherein the variables of Formula (I) are defined herein. This disclosure also provides pharmaceutical compositions comprising the compounds, uses of the compounds, and compositions for treatment of, for example, a metabolic or cardiovascular disorder. Further, the disclosure provides intermediates useful in the synthesis of compounds of Formula (I).

Regioselective SNAr reactions of substituted difluorobenzene derivatives: practical synthesis of fluoroaryl ethers and substituted resorcinols

Ouellet, Stéphane G.,Bernardi, Anna,Angelaud, Remy,O'Shea, Paul D.

supporting information; experimental part, p. 3776 - 3779 (2009/10/11)

In this Letter, we describe a practical and highly selective method for the preparation of fluoroaryl ethers and differentially substituted resorcinol derivatives. This synthetic strategy relies on a selective SNAr of substituted difluorobenzen

Regioselectivity of fluorine substitution by alkoxides on unsymmetrical difluoroarenes

Dirr, Ronan,Anthaume, Cyril,Désaubry, Laurent

, p. 4588 - 4590 (2008/09/21)

An efficient approach to unsymmetrical halogenated resorcinol diethers has been developed. This synthesis consists of two subsequent nucleophilic aromatic substitutions (SNAr) of unsymmetrical difluoroarenes by alkoxides. The novelty of this ap

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