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Phenyl-2-aminobenzenesulfonate, also known as 2-aminobenzenesulfonic acid phenyl ester, is an aromatic sulfonate compound with the molecular formula C12H11NO3S. It is a derivative of phenylamine and sulfonic acid, commonly used in the synthesis of pharmaceuticals and organic synthesis. This versatile chemical compound is often utilized as a reagent in various chemical reactions and has a wide range of applications, including as an intermediate in the production of dyes, pigments, and other organic compounds. Additionally, it exhibits potential pharmacological properties and is being studied for its potential biological activities.

68227-69-0

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68227-69-0 Usage

Uses

Used in Pharmaceutical Synthesis:
Phenyl-2-aminobenzenesulfonate is used as an intermediate in the synthesis of various pharmaceuticals for its ability to facilitate the formation of complex organic molecules, contributing to the development of new drugs and therapeutic agents.
Used in Organic Synthesis:
As a reagent in organic synthesis, Phenyl-2-aminobenzenesulfonate is used for its capacity to participate in a variety of chemical reactions, aiding in the creation of diverse organic compounds.
Used in Dye and Pigment Production:
Phenyl-2-aminobenzenesulfonate is used as an intermediate in the production of dyes and pigments, enabling the creation of a broad spectrum of colors for various applications in industries such as textiles, plastics, and printing.
Used in Research and Development:
In the field of research and development, Phenyl-2-aminobenzenesulfonate is used to explore its potential pharmacological properties and biological activities, with the aim of discovering new applications in medicine and other fields.
Used in Chemical Reactions:
Phenyl-2-aminobenzenesulfonate is utilized as a reagent in various chemical reactions, playing a crucial role in the synthesis of a wide array of organic compounds, thus contributing to the advancement of chemical science and technology.

Check Digit Verification of cas no

The CAS Registry Mumber 68227-69-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,2,2 and 7 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 68227-69:
(7*6)+(6*8)+(5*2)+(4*2)+(3*7)+(2*6)+(1*9)=150
150 % 10 = 0
So 68227-69-0 is a valid CAS Registry Number.
InChI:InChI=1/C12H11NO3S/c13-11-8-4-5-9-12(11)17(14,15)16-10-6-2-1-3-7-10/h1-9H,13H2

68227-69-0 Well-known Company Product Price

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  • Aldrich

  • (539597)  Phenyl-2-aminobenzenesulfonate  97%

  • 68227-69-0

  • 539597-5G

  • 321.75CNY

  • Detail
  • Aldrich

  • (539597)  Phenyl-2-aminobenzenesulfonate  97%

  • 68227-69-0

  • 539597-25G

  • 1,269.45CNY

  • Detail

68227-69-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name Phenyl-2-aminobenzenesulfonate

1.2 Other means of identification

Product number -
Other names phenyl 2-aminobenzenesulfonate

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:68227-69-0 SDS

68227-69-0Downstream Products

68227-69-0Relevant articles and documents

Catalysis of Sulfonate Ester Hydrolysis by Intramolecular Amide Group Assistance.

Thea, Sergio,Guanti, Giuseppe,Hopkins, Andrew R.,Williams, Andrew

, p. 3336 - 3341 (2007/10/02)

Kinetics of the alkaline hydrolysis of aryl 2-(acylamino)benzenesulfonates (1, X=OAr) obey the equation kobs=(Ka+kb->/(1++>/Ko).Hammett equations correlate the parameters ka, kb, and Ka for variation in both amido and leaving phenolate substituents.The values and sign of the ρ values together with entropy of activation data, reactivity trapping, and oxygen-18 incorporation are consistent with the formation of an intermediate benzoxathiazine S,S-dioxide (2).The ka term involves intramolecular attack of the amido anion.The kb term is consistent with a specific anion effect on ka.Regular bimolecular BAc2 mechanisms for ka and kb are not consistent with the high observed reactivity of these parameters.

The Pyrolysis of 2-Azidobenzoates. A New Synthesis of Carbazoles and Other N-Heterocycles

Clancy, Michael G.,Hesabi, Massoud M.,Meth-Cohn, Otto

, p. 429 - 434 (2007/10/02)

The spray pyrolysis of aryl 2-azidobenzoates yields carbazoles, involving a rearrangement whereby the nitrogen of the product is attached to the aryl 1-carbon, a process involving a spiro 6-membered intermediate.When the aryl ortho-positions were both alkyl substituted the product was ab acridan instead.With an ortho-carboxylate, acridone formation competed with that of carbazole.When the CO-O group of the substrate was replaced by O-CO, CO-S, CO-NPh, or SO2-O the pyrolysis was ineffective.Benzyl 2-azidobenzoates, however, pyrolysed to yield 1-benzyl-2,1-benzisoxazolones by an unprecedented C-O insertion reaction of the intermediate nitrene.

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