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1-(4-chlorophenyl)-2,2,3,3,3-pentafluoropropan-1-ol is a synthetic organic compound characterized by its unique molecular structure. It features a 1-hydroxypropan-2-yl backbone, with one of the carbon atoms bearing a hydroxyl group. The molecule is further distinguished by the presence of a 4-chlorophenyl group attached to the first carbon, which introduces a chlorine atom at the para position of the phenyl ring. Additionally, the molecule contains five fluorine atoms attached to the second carbon of the propane chain, making it a highly fluorinated compound. This chemical is known for its potential applications in pharmaceuticals and agrochemicals, particularly as an intermediate in the synthesis of various active ingredients. Its specific properties, such as reactivity and stability, are influenced by the presence of the chlorine and fluorine atoms, which can affect its electronic and steric characteristics.

1579-58-4

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1579-58-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1579-58-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,7 and 9 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1579-58:
(6*1)+(5*5)+(4*7)+(3*9)+(2*5)+(1*8)=104
104 % 10 = 4
So 1579-58-4 is a valid CAS Registry Number.

1579-58-4Relevant academic research and scientific papers

Pentafluoroethyl group containing production of alcohols, organic semiconductor material and intermediate compound of the enzyme activity inhibitor

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Paragraph 0057-0059; 0066-0068, (2021/10/15)

[A] a pharmaceutical, agrochemical, a pentafluoroethyl group containing alcohol compound useful as a method for producing polymeric functional materials, as well as, organic semiconductor material and enzyme activity inhibitor of the intermediate compound

A Facile Stereoselcetive Synthesis of (E)-1-Aryl-1,2,3,3,3-pentafluoropropenes and (E)-1-Aryl-2-chloro-1,3,3,3-tetrafluoropropenes

Kuroboshi, Manabu,Hiyama, Tamejiro

, p. 1607 - 1610 (2007/10/02)

Arenecarbaldehydes ArCHO were allowed to react with a carbenoid reagent CF3CX2Mtl (X=Cl, Mtl=ZnCl, X=F, Mtl=LI) to give the adducts ArCH(OH)CX2CF3 whose hydroxyl group was substituted by fluorine.Dehydrohalogenating of the resultant ArCHFCX2CF3 (X=Cl or F

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