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4-[(4-fluorophenyl)sulfonyl]phenol is an organic compound characterized by its molecular formula C12H9FO3S. This chemical features a phenol group (a hydroxyl group attached to a benzene ring) with a sulfonyl group (-SO2-) attached to the para position of the phenol's benzene ring. The sulfonyl group is further connected to a 4-fluorophenyl group, which introduces a fluorine atom at the para position of the phenyl ring. 4-[(4-fluorophenyl)sulfonyl]phenol is known for its potential applications in the synthesis of pharmaceuticals and other organic compounds, where its unique structure can influence reactivity and properties. It is important to handle such chemicals with care due to their potential reactivity and to follow appropriate safety protocols.

312-36-7

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312-36-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 312-36-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,1 and 2 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 312-36:
(5*3)+(4*1)+(3*2)+(2*3)+(1*6)=37
37 % 10 = 7
So 312-36-7 is a valid CAS Registry Number.

312-36-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(4-fluorophenyl)sulfonylphenol

1.2 Other means of identification

Product number -
Other names 4-(4-Fluor-phenylsulfon)-phenol

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:312-36-7 SDS

312-36-7Relevant academic research and scientific papers

One-step hydroxylation of aryl and heteroaryl fluorides using mechanochemistry

Braje, Wilfried,Geneste, Hervé,Rodrigo, Eduardo,Walter, Magnus W.,Wiechert, Rainer

supporting information, p. 1469 - 1473 (2022/03/07)

Simple use of KOH allows the direct F to OH exchange of aromatic and heteroaromatic substrates under mechanochemical conditions. The reaction is performed in the absence of solvent with potassium hydroxide as OH source. As a result, this approach is both more atom economical and environmentally friendly than previously described methods for this transformation.

Modulation of Thermally Activated Delayed Fluorescence in Waterborne Polyurethanes via Charge-Transfer Effect

Li, Zongren,Wang, Tao,Xu, Dong,Zuo, Jie,Li, Xinyu,Li, Zhiwei,Xu, Fei,Zhang, Xingyuan

, p. 2302 - 2308 (2019/06/17)

Here, we designed several waterborne polyurethanes (WPUs) with efficient thermally activated delayed fluorescence (TADF) via serving charge-transfer (CT) states as a mediate bridge between singlet and triplet states to boost reverse intersystem crossing (RISC). By tuning substituents of diphenyl sulfone (DS), we found that O,O′- and S,S′-substituted DS covalently incorporated in WPUs solely show typical fluorescence emission with lifetimes in the nanosecond range. Interestingly, TADF appears by replacing the substituent with the nitrogen atom, of which lifetimes are up to ≈10 microseconds and ≈1 millisecond in air and vacuum, respectively, even though the energy gap between singlet and triplet states (ΔEST) is still large for generating TADF. To explain this phenomenon, an energy level mode based on CT states and an 3(n-π*) receiver state was proposed. By the rational modulation of CT states, it is possible to tune the ΔEST to render TADF-based materials suitable for versatile applications.

ION TRANSFER COMPOUND

-

Paragraph 0082-0083, (2017/05/23)

The present invention relates to an ion transfer compound. According to an embodiment of the present invention, the compound contains three or more ion transfer functional groups, and may have high ion conductivity.COPYRIGHT KIPO 2017

Well-defined star-shaped rod-coil diblock copolymers as a new class of unimolecular micelles: Encapsulation of guests and thermoresponsive phase transition

Park, Jeyoung,Moon, Mihee,Seo, Myungeun,Choi, Hyungsam,Kim, Sang Youl

experimental part, p. 8304 - 8313 (2011/12/15)

A series of star-shaped rod-coil diblock copolymers composed of poly(arylene ether sulfone) (PAES) as a core, and poly[2-(2-methoxyethoxy)ethyl methacrylate-co-oligo(ethylene glycol) methacrylate] [poly(MEO 2MA-co-OEGMA)] as a shell was synthes

Heat-sensitive recording material

-

, (2008/06/13)

A heat-sensitive recording material which comprises in its color reactant system, as developer for the color former, at least one aluminum or zinc phenate of a phenolsulfonyl compound of the formula STR1 wherein R is C1 -C12 alkyl, cycloalkyl, phenyl, benzyl, or phenyl which is substituted by halogen, lower alkyl, lower alkoxy, nitro or methylenedioxy, and X is hydrogen, halogen, lower alkyl or lower alkoxy.

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