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Dibenzofuran-2-sulfonic acid, with the molecular formula C12H10O4S, is a white crystalline powder that exhibits solubility in organic solvents but not in water. This chemical compound serves as a versatile reagent in chemical reactions and a fundamental building block in the synthesis of a range of products, including pharmaceuticals, dyes, and other organic compounds. Its applications extend to environmental and industrial uses, such as wastewater treatment and corrosion inhibition, as well as in the realm of analytical chemistry as a pH indicator and in the production of fluorescent dyes.

83863-63-2

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83863-63-2 Usage

Uses

Used in Pharmaceutical Synthesis:
Dibenzofuran-2-sulfonic acid is used as a key intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of novel drug molecules with potential therapeutic properties.
Used in Dye Production:
In the dye industry, Dibenzofuran-2-sulfonic acid is utilized as a building block for the creation of various dyes, capitalizing on its chemical structure to produce a spectrum of colorants for different applications.
Used in Wastewater Treatment:
Dibenzofuran-2-sulfonic acid is employed as a component in the treatment of wastewater, potentially aiding in the removal of pollutants and contributing to environmental remediation efforts.
Used as a Corrosion Inhibitor:
In industrial settings, DIBENZOFURAN-2-SULFONIC ACID serves as a corrosion inhibitor, protecting materials from the damaging effects of corrosive agents and extending the lifespan of equipment and structures.
Used in Analytical Chemistry as a pH Indicator:
Dibenzofuran-2-sulfonic acid is used as a pH indicator, leveraging its chemical properties to signal changes in acidity or alkalinity in various solutions.
Used in the Production of Fluorescent Dyes:
DIBENZOFURAN-2-SULFONIC ACID is also utilized in the creation of fluorescent dyes, where its unique properties allow for applications in fields such as bioimaging and diagnostics, where the visibility of specific markers or structures is crucial.

Check Digit Verification of cas no

The CAS Registry Mumber 83863-63-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,8,6 and 3 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 83863-63:
(7*8)+(6*3)+(5*8)+(4*6)+(3*3)+(2*6)+(1*3)=162
162 % 10 = 2
So 83863-63-2 is a valid CAS Registry Number.
InChI:InChI=1/C12H8O4S/c13-17(14,15)8-5-6-12-10(7-8)9-3-1-2-4-11(9)16-12/h1-7H,(H,13,14,15)/p-1

83863-63-2 Well-known Company Product Price

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  • Alfa Aesar

  • (43899)  Dibenzofuran-2-sulfonic acid hydrate, 97%   

  • 83863-63-2

  • 1g

  • 688.0CNY

  • Detail

83863-63-2SDS

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 Dibenzo[b,d]furan-2-sulfonic acid

1.2 Other means of identification

Product number -
Other names DIBENZOFURAN-2-SULFONIC ACID

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:83863-63-2 SDS

83863-63-2Upstream product

83863-63-2Relevant academic research and scientific papers

Synthesis and biological activity of various derivatives of a novel class of potent, selective, and orally active prostaglandin D2 receptor antagonists. 1. Bicyclo[2.2.1]heptane derivatives

Mitsumori, Susumu,Honma, Tsunetoshi,Tsuri, Tatsuo,Hiramatsu, Yoshiharu,Okada, Toshihiko,Hashizume, Hiroshi,Inagaki, Masanao,Arimura, Akinori,Yasui, Kiyoshi,Asanuma, Fujio,Kishino, Junji,Ohtani, Mitsuaki

, p. 2436 - 2445 (2007/10/03)

Novel prostaglandin D2 (PGD2) receptor antagonists were synthesized as a potential new class of antiallergic agents having a bicyclo[2.2.1] heptane ring system with sulfonamide groups. Some of them exhibit extremely potent antagonism of the PGD2 receptor in radioligand binding and cAMP formation assays with IC50 values below 50 nM and much less antagonism of TXA2 and PGI2 receptors. These potent PGD2 receptor antagonists, when given orally, dramatically suppress various allergic inflammatory responses such as increased vascular permeability in allergic rhinitis, conjunctivitis, and asthma models. The excellent pharmacological profiles of PGD2 receptor antagonists, originally synthesized in our laboratories, are of potentially great clinical significance. This study also provides experimental evidence suggesting that PGD2 plays an important role in the pathogenesis of allergic diseases.

Highly selective and orally active inhibitors of type IV collagenase (MMP-9 and MMP-2): N-sulfonylamino acid derivatives

Tamura, Yoshinori,Watanabe, Fumihiko,Nakatani, Takuji,Yasui, Ken,Fuji, Masahiro,Komurasaki, Tadafumi,Tsuzuki, Hiroshige,Maekawa, Ryuji,Yoshioka, Takayuki,Kawada, Kenji,Sugita, Kenji,Ohtani, Mitsuaki

, p. 640 - 649 (2007/10/03)

Various N-sulfonylamino acid derivatives were synthesized and evaluated for their in vitro and in vivo activities to inhibit type IV collagenase (MMP-9 and MMP-2). When the amino acid residue and the sulfonamide moiety were modified, their inhibitory activities were greatly affected by the structure of the sulfonamide moiety. A series of aryl sulfonamide derivatives containing biaryl, tetrazole, amide, and triple bond were found to be potent and highly selective inhibitors of MMP-9 and MMP-2. In addition, these compounds were orally active in animal models of tumor growth and metastasis. These results revealed the potential of the N-sulfonylamino acid derivatives as a new type of candidate drug for the treatment of cancer.

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