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2,4,6-tris(chlorosulfonyl)phenol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

858013-34-0

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858013-34-0 Usage

Chemical structure

A phenolic compound with three chlorosulfonyl functional groups attached to the phenol ring.

Reactivity

Highly reactive chemical compound.

Use

Used as a precursor in the synthesis of a wide range of organic compounds.

Functional groups

Chlorosulfonyl groups.

Electrophilicity

Strong electrophile due to the presence of chlorosfonyl groups.

Applications

Utilized in the production of dyes, pharmaceuticals, and agrochemicals. Also used in the manufacturing of high-performance polymers and resins.

Toxicity

Highly toxic.

Corrosiveness

Corrosive.

Safety precautions

Can cause severe skin and eye irritation. Proper handling and safety precautions are necessary when working with 2,4,6-tris(chlorosulfonyl)phenol.

Check Digit Verification of cas no

The CAS Registry Mumber 858013-34-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,8,0,1 and 3 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 858013-34:
(8*8)+(7*5)+(6*8)+(5*0)+(4*1)+(3*3)+(2*3)+(1*4)=170
170 % 10 = 0
So 858013-34-0 is a valid CAS Registry Number.

858013-34-0Upstream product

858013-34-0Relevant academic research and scientific papers

A convenient synthetic route to 2,4,6-tris(chlorosulfonyl)- and 2,4,6-tris(fluorosulfonyl)phenol, aniline and chlorobenzene

Boiko, Vladimir N.,Filatov, Andrey A.,Yagupolskii, Yurii L.,Tyrra, Wieland,Naumann, Dieter,Pantenburg, Ingo,Fischer, Hendrik T.M.,Schulz, Frank

experimental part, p. 1219 - 1226 (2011/11/30)

Convenient and preparative synthetic procedures of 2,4,6- tris(chlorosulfonyl)- and 2,4,6-tris(fluorosulfonyl)phenol, -chlorobenzene and -aniline have been elaborated. Chlorine exchange for fluorine by KF interaction on 2,4,6-tris(chlorosulfonyl)aniline and especially 2,4,6-tris(chlorosulfonyl) phenol proceeds easily and selectively under anhydrous conditions in dioxane. Unlike, 2,4,6-tris(chlorosulfonyl)chlorobenzene transformation requires the presence of water. On the basis of 2,4,6-tris(fluorosulfonyl)phenol and some of its salts, XRD measurements demonstrated the structural similarity to picric acid and its derivatives in the solid state.

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