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4-Hydroxyphenyl trifluoromethyl sulphone, also known as 4-Hydroxyphenyl trifluoromethanesulfone, is a chemical compound with the molecular formula C7H5F3O3S. It is a white crystalline solid that is soluble in organic solvents and has a melting point of approximately 90-92°C. 4-Hydroxyphenyl trifluoromethyl sulphone is an important intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. It is also used as a building block in the preparation of various functional materials, such as polymers and dyes. Due to its unique structure, it exhibits interesting properties, such as high thermal stability and chemical reactivity, making it a valuable compound in the field of organic chemistry and material science.

432-84-8

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432-84-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 432-84-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,3 and 2 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 432-84:
(5*4)+(4*3)+(3*2)+(2*8)+(1*4)=58
58 % 10 = 8
So 432-84-8 is a valid CAS Registry Number.

432-84-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(trifluoromethylsulfonyl)phenol

1.2 Other means of identification

Product number -
Other names 4-Trifluoromethanesulfonyl-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:432-84-8 SDS

432-84-8Relevant academic research and scientific papers

COMPOSITES, METHODS AND USES THEREOF

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Page/Page column 26, (2021/06/04)

The present invention relates, in general terms, to methods of catalysing a reaction, including the steps of contacting a chemical entity comprising a sulphide moiety with a composite and an oxidant. The composite acts as a heterogeneous catalyst to oxidise the sulphide moiety. The present invention also relates to composites, methods of synthesising the composites and its use as a catalyst thereof.

METHOD FOR PRODUCING 4-(TRIFLUOROMETHYLSULFONYL)PHENOL COMPOUND

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Paragraph 0048; 0049; 0050; 0051; 0052; 0054; 0055; 0060, (2018/07/29)

A compound represented by formula (4): can be produced by adding a heterogeneous transition metal catalyst to a solution containing a compound represented by formula (3): obtained by performing a nitration reaction by adding a nitrating agent to a solution containing a compound represented by formula (2): obtained by oxidizing a compound represented by formula (1): with hydrogen peroxide in the presence of sodium tungstate and a saturated C8 carboxylic acid, then adding water to the resultant mixture, and separating the resultant solution.

METHOD FOR PRODUCING PHENOLIC COMPOUND

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Paragraph 0052; 0053, (2017/06/12)

Provided is a method for producing a compound represented by formula (2-b), which is useful as an intermediate for producing agricultural chemicals. The method includes a step for obtaining a compound represented by formula (2-a) by oxidizing the compound represented by formula (1) with hydrogen peroxide in the presence of sulfuric acid and/or a C1-6 alkanesulfonic acid that may be halogen-substituted and in the presence of a C2-12 aliphatic carboxylic acid and/or sulfolane. The method also includes a step for obtaining a compound represented by formula (2-b) by nitrating a compound represented by formula (2-a) in the presence of sulfuric acid and/or a C1-6 alkanesulfonic acid that may be halogen-substituted.

NOVEL SILANE COMPOUND HAVING SULFONE STRUCTURE

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Paragraph 0121, (2017/01/26)

PROBLEM TO BE SOLVED: To provide a silane compound useful for the production of a semiconductor device. SOLUTION: The present invention provides a compound represented by formula (5) [R2 is alkoxy, acyloxy or halogen; a is 1; R3 is a group represented by formula (6) (one of R4-R6 and Ar1-Ar2 bonds to an Si atom by an Si-C bond; R4 and R6 independently represent a monovalent-tetravalent hydrocarbon; R5 is a divalent-tetravalent hydrocarbon; Ar1 and Ar2 are a substituted/unsubstituted phenyl or phenylene group; n2 is 1; n1, n3-n5 independently represent 0 or 1)]. SELECTED DRAWING: None COPYRIGHT: (C)2017,JPOandINPIT

FUSED OXAZOLE COMPOUNDS AND USE THEREOF FOR PEST CONTROL

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Page/Page column 110; 111, (2014/07/21)

Disclosed is a compound represented by formula (1): wherein A1 represents N(O)p or CH; A2 represents N(O)q; R1 represents a trifluoromethyl group, a halogen atom or a hydrogen atom; R2 represents a C1-C3 perfluoroalkyl group, p represents 0 or 1; q represents 0 or 1; n represents 0, 1 or 2; and m represents 0, 1 or 2, having an excellent controlling effect on pests.

MODULATORS OF DOPAMINE NEUROTRANSMISSION

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Page/Page column 57, (2009/12/05)

The present invention relates to novel 1-(2,3-dihydro-1,4-benzodioxin-2-yl)- methanamine derivatives, useful as modulators of dopamine neurotransmission, and more specifically as dopaminergic stabilizers. In other aspects the invention relates to the use of these compounds in a method for therapy and to pharmaceutical compositions comprising the compounds of the invention.

ELECTROLYTE MATERIALS CONTAINING HIGHLY DISSOCIATED METAL ION SALTS

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, (2008/06/13)

The present invention relates to metal ion salts which can be used in electrolytes for producing electrochemical devices, including both primary and secondary batteries, photoelectrochemical cells and electrochromic displays. The salts have a low energy o

PREPARATION AND FLUORINATION OF ARYLTRIFLUOROMETHYLSULPHONES

Beaumont, Andrew J.,Clark, James H.

, p. 295 - 300 (2007/10/02)

A series of chloro- and nitrophenyl trifluoromethyl sulphides and sulphones have been synthesised from the corresponding aryl halides .The fluorination of these compounds by tetra-n-butyl ammonium fluoride and potassium fluoride has been investigated.Our results show that generally they are more susceptible to fluorodenitration than fluorodechlorination.

Novel benzopyran derivatives, processes for their preparation and their use and preparations containing the compounds

-

, (2008/06/13)

Benzopyran derivatives of the general formula I STR1 are disclosed. The compounds are therapeutic active compounds.

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