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23156-75-4

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23156-75-4 Usage

Description

2-(Phenylsulfonyl)-1,4-benzenediol, also known as 2-Hydroxy-5-(phenylsulfonyl)benzaldehyde, is a synthetic chemical compound with the molecular formula C13H10O5S. It is commonly classified as a benzene and its derivatives, and falls under the organosulfur compounds category. 2-(PHENYLSULFONYL)-1,4-BENZENEDIOL is characterized by its unique structure and properties, which can be analyzed using techniques such as NMR spectroscopy, IR Spectroscopy, and mass spectrometry.

Uses

Used in Organic Chemistry Research:
2-(Phenylsulfonyl)-1,4-benzenediol is used as a research compound in the field of organic chemistry. It serves as a valuable tool for various experimental applications, contributing to the advancement of chemical knowledge and understanding.
Used as an Intermediate in Chemical Reactions:
In the realm of chemical synthesis, 2-(Phenylsulfonyl)-1,4-benzenediol is employed as an intermediate. Its unique structure allows it to participate in a range of chemical reactions, facilitating the production of other compounds.
Used as a Catalyst in Chemical Reactions:
2-(Phenylsulfonyl)-1,4-benzenediol also serves as a catalyst in certain chemical reactions. Its presence can enhance the rate and efficiency of these processes, making it a useful component in the synthesis of various compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 23156-75-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,1,5 and 6 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 23156-75:
(7*2)+(6*3)+(5*1)+(4*5)+(3*6)+(2*7)+(1*5)=94
94 % 10 = 4
So 23156-75-4 is a valid CAS Registry Number.
InChI:InChI=1/C12H10O4S/c13-9-6-7-11(14)12(8-9)17(15,16)10-4-2-1-3-5-10/h1-8,13-14H

23156-75-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(benzenesulfonyl)benzene-1,4-diol

1.2 Other means of identification

Product number -
Other names 2-phenylsulfonyl-1,4-dihydroxybenzene

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:23156-75-4 SDS

23156-75-4Relevant articles and documents

Different strategies in electrochemical synthesis of new mono and di-substituted hydroquinone and benzoquinone

Nematollahi, Davood,Momeni, Shima,Khazalpour, Sadegh

, p. 310 - 318 (2014)

Electrochemical syntheses of 2-indolyl-5-arylsulfonyl-p-benzoquinone derivatives were carried out in two successive oxidation steps. The first involves the oxidation of hydroquinone, 4-(piperazin-1-yl) phenol) and 1-(4-(4-hydroxyphenyl) piperazin-1-yl) et

Electrochemical-In-Situ-Oxidative Sulfonylation of Phenols with Sulfinic Acids as an Access to Sulfonylated Hydroquinones

Sun, Xue,Zhang, Fanjun,Yan, Kelu,Feng, Wenfeng,Sun, Xuejun,Yang, Jianjing,Wen, Jiangwei

supporting information, p. 3485 - 3490 (2021/06/17)

The electrochemical in-situ oxidative sulfonylation of phenols with sulfinic acids access to sulfonylated hydroquinones has been developed. A series of sulfonylated hydroquinones were prepared under mild mediator-, catalyst- and exogenous-oxidant-free con

Bisketene Equivalents as Diels-Alder Dienes

Dissanayake, Isuru,Hart, Jacob D.,Becroft, Emma C.,Sumby, Christopher J.,Newton, Christopher G.

supporting information, p. 13328 - 13333 (2020/09/03)

2,5-Bis(tert-butyldimethylsilyloxy)furans are established as vicinal bisketene equivalents for application as dienes in the Diels-Alder reaction. Cycloaddition with olefinic dienophiles, under exceptionally mild conditions, enables convergent access to highly substituted para-hydroquinones in unprotected form via a one-pot Diels-Alder/ring-opening/tautomerization sequence. The synthesis of para-benzoquinones from acetylenic dienophiles, including benzynes, is also demonstrated, and 2,5-bis(tert-butyldimethylsilyloxy)pyrroles are established as competent dienes for the synthesis of para-iminoquinones. Application in natural product synthesis enables gram-scale access to the neuroprotective agent (±)-indanostatin.

Preparation method for sulfonyl hydroquinone compound

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Paragraph 0065; 0066; 0067, (2017/04/29)

The invention belongs to the field of organic synthesis, and in particular, relates to a preparation method for a sulfonyl hydroquinone compound. According to the preparation method, a cheap and easily obtained quinone compound is used as a raw material, stable and easy-to-preserve sulfonyl hydrazide is used as a sulfonylation reagent, metal-free catalysis is adopted, reaction conditions are environmentally friendly, the preparation process is simplified, and the yield is increased.

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