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2-Fluoro-benzenesulfonic acid is a chemical compound characterized by the molecular formula C6H5FO3S. It is a derivative of benzenesulfonic acid, distinguished by the presence of a fluorine atom attached to the benzene ring. This colorless liquid is recognized for its strong acidic properties and corrosive nature, necessitating careful handling and adherence to safety protocols to prevent skin and eye burns.

35300-35-7

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35300-35-7 Usage

Uses

Used in Organic Synthesis:
2-Fluoro-benzenesulfonic acid serves as a reagent in organic synthesis, facilitating various chemical reactions due to its strong acidic character. It is particularly valuable for its ability to participate in reactions that require the introduction or modification of fluorine-containing groups in organic molecules.
Used in Pharmaceutical Production:
As an intermediate, 2-Fluoro-benzenesulfonic acid plays a crucial role in the production of pharmaceuticals. Its unique chemical properties make it suitable for the synthesis of a range of medicinal compounds, contributing to the development of new drugs and therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical sector, 2-Fluoro-benzenesulfonic acid is utilized as an intermediate in the synthesis of various agrochemicals. Its application aids in the development of effective pesticides, herbicides, and other agricultural chemicals that are essential for crop protection and yield enhancement.
Used in Dye Manufacturing:
2-Fluoro-benzenesulfonic acid is also employed in the manufacturing of dyes, where its chemical structure contributes to the creation of vibrant and stable colorants used in various industries, including textiles, plastics, and printing.
Used in Polymer Production:
2-Fluoro-benzenesulfonic acid finds application in the production of polymers, where it may be used to modify polymer properties or as a component in the synthesis of specialty polymers with unique characteristics, such as enhanced stability or specific interaction profiles.
Used in Specialty Chemicals Synthesis:
Finally, 2-Fluoro-benzenesulfonic acid is utilized in the synthesis of specialty chemicals, which are high-value compounds used in niche applications across various industries, from advanced materials to environmental and analytical chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 35300-35-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,3,0 and 0 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 35300-35:
(7*3)+(6*5)+(5*3)+(4*0)+(3*0)+(2*3)+(1*5)=77
77 % 10 = 7
So 35300-35-7 is a valid CAS Registry Number.

35300-35-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Fluorobenzenesulfonic acid

1.2 Other means of identification

Product number -
Other names 2-Fluoro-benzenesulfonic 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:35300-35-7 SDS

35300-35-7Downstream Products

35300-35-7Relevant academic research and scientific papers

HYDROLYSIS OF AROMATIC SULFONIC ACIDS UNDER THERMODYNAMIC CONTROL OF THE REACTION

Krylov, E. N.,Volgina, L. V.,Isaeva, G. Yu.

, p. 1129 - 1133 (2007/10/02)

Linear mathematical models which describe the hydrolysis of alkyl- and halobenzenesulfonyl acids under the conditions for their isomerization in sulfuric acid have been obtained by the method of mathematical experiment planning.The value of the effective rate constants of hydrolysis calculated according to the models for comparative conditions (150 deg C, 3 moles of 85percent sulfuric acid) were used to obtain the correlation between log kh and the ? constants of the substituents.The correlation corresponds the electrophilic nature of the hydrolysis process (ρ = -4.69).The strong influence of the electronic effects of the substituents on the rate of hydrolysis is an indication of the development of a considerable positive charge on the reaction center in the transition state.

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