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Hydroquinone ditosylate, also known as 4-tosyloxyaniline, is a chemical compound with the molecular formula C13H13NO3S. It is a derivative of hydroquinone, where one of the hydroxyl groups is replaced by a tosyl group (a toluene sulfonate group). This modification enhances the solubility and reactivity of the compound, making it useful in various chemical reactions and as an intermediate in the synthesis of other organic compounds. Hydroquinone ditosylate is particularly employed in the preparation of dyes, pharmaceuticals, and other specialty chemicals. It is also known for its use in the protection of phenols and the synthesis of aryl ethers. Due to its reactivity, it is important to handle hydroquinone ditosylate with care, following proper safety protocols.

2581-43-3

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2581-43-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2581-43-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,8 and 1 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2581-43:
(6*2)+(5*5)+(4*8)+(3*1)+(2*4)+(1*3)=83
83 % 10 = 3
So 2581-43-3 is a valid CAS Registry Number.
InChI:InChI=1/C20H18O6S2/c1-15-3-11-19(12-4-15)27(21,22)25-17-7-9-18(10-8-17)26-28(23,24)20-13-5-16(2)6-14-20/h3-14H,1-2H3

2581-43-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name HYDROQUINONE DITOSYLATE

1.2 Other means of identification

Product number -
Other names 1,4-dicarboxybenzene

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:2581-43-3 SDS

2581-43-3Relevant academic research and scientific papers

Ionic liquid brush as an efficient and reusable heterogeneous catalytic assembly for the tosylation of phenols and alcohols in neat water

Feng, Simin,Li, Jing,Wei, Junfa

supporting information, p. 4743 - 4746 (2017/07/12)

A very efficient and reusable heterogeneous ionic liquid brush assembly was developed. The catalyst exhibits high catalytic activity for the tosylation of phenols and alcohols in neat water. Moreover, the catalyst shows outstanding stability and reusability, and it can be simply and effectively recovered and reused five times without noticeable loss of catalytic activity.

Chromatography-Free and Eco-Friendly Synthesis of Aryl Tosylates and Mesylates

Lei, Xiangyang,Jalla, Anusha,Abou Shama, Mhd A.,Stafford, Jamie M.,Cao, Billy

supporting information, p. 2578 - 2585 (2015/09/01)

Two chromatography-free and eco-friendly protocols have been developed to synthesize aryl tosylates and mesylates by the tosylation and mesylation of the corresponding hydroxyarenes, respectively. These protocols are superior to other known ones regarding

Triazole-pyridine ligands: A novel approach to chromophoric iridium arrays

Juriek, Michal,Felici, Marco,Contreras-Carballada, Pablo,Lauko, Jan,Bou, Sandra Rodriguez,Kouwer, Paul H. J.,Brouwer, Albert M.,Rowan, Alan E.

supporting information; experimental part, p. 2104 - 2111 (2011/10/02)

We describe a novel modular approach to a series of luminescent iridium complexes bearing triazole-pyridine-derived ligands that were conveniently prepared by using "click" chemistry. One, two or three triazole-pyridine units were effectively built into the heteroaromatic macromolecule using versatile acetylene- and azide-functionalised precursors. Using this approach, a series of iridium-derived molecules, that differ in the number of iridium centres, the structural characteristics of the cyclometalating ligand and the backbone, were synthesised. The preliminary photophysical properties of the prepared complexes indicate that there is only limited interaction (through space or through the backbone) between the iridium centres within one molecule and that each iridium centre retains its individual properties. The results show that our approach can be generally applied towards covalently linked multichromophoric systems with potential application, for instance, in the design and preparation of tunable light emitters. As a demonstration of this concept, a single molecule white-light emitter, constructed from two iridium centres (yellow emission) and a fluorene unit (blue emission), is presented. The Royal Society of Chemistry.

Graphite/methanesulfonic acid (GMA) as a new reagent for sulfonylation of phenols and thia-Fries rearrangement of aryl sulfonates to sulfonylphenols

Sharghi, Hashem,Shahsavari-Fard, Zahra

, p. 42 - 52 (2007/10/03)

A new facile method for direct sulfonylation of phenols was developed. Graphite in methanesulfonic acid (GMA) was used to prepare sulfonylphenols by sulfonylation of phenol and naphthalene derivatives with p-toluenesulfonic acid (=4-methylbenzenesulfonic acid) (Table 1) and the thia-Fries rearrangement of aryl sulfonates (Table 4). Mechanistic studies showed that the sulfonylation reaction of phenols in GMA occurred through an initial sulfonate formation followed by a thia-Fries rearrangement of the aryl sulfonate by an intermolecular mechanism (Scheme 3).

Selected sulfonyl compounds as anticancer/antimalarial agents

Langler, Richard F.,Paddock, Robert L.,Thompson, David B.,Crandall, Ian,Ciach, Michelle,Kain, Kevin C.

, p. 1127 - 1133 (2007/10/03)

The synthesis and biological testing of a series of sulfonyl phenols and sulfonyl aryl methyl ethers has revealed that p-methoxyphenyl p-toluenesulfonate is a very selective and effective antimalarial agent which shows pronounced activity against human skin cancer cells. Application of a counter-attack strategy permits the direct preparation of the requisite tosylate ether from the bis(tosylate) of dihydroquinone.

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