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6-Chloropyridine-3-sulfonic acid, with the molecular formula C5H4ClNO3S, is a sulfonic acid derivative of pyridine. It features a pyridine ring with a chlorine atom and a sulfonic acid group at the 3-position, making it a versatile building block in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals. This water-soluble compound is typically handled and stored as a solid, requiring careful handling and adherence to safety protocols due to its potential hazards.

17624-08-7

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17624-08-7 Usage

Uses

Used in Pharmaceutical Industry:
6-Chloropyridine-3-sulfonic acid is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to be incorporated into complex molecular structures, contributing to the development of new drugs with specific therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical sector, 6-chloropyridine-3-sulfonic acid is utilized as a building block for the creation of agrochemicals, such as pesticides and herbicides, due to its reactivity and potential to form stable and effective compounds.
Used in Specialty Chemicals Industry:
6-Chloropyridine-3-sulfonic acid is employed as a precursor in the production of specialty chemicals, where its unique chemical structure allows for the development of compounds with specific applications in various industries, such as dyes, coatings, and materials science.
Used as a Reagent in Organic Synthesis:
6-Chloropyridine-3-sulfonic acid serves as a reagent in organic synthesis, facilitating various chemical reactions and transformations, which are essential for the production of a wide range of organic compounds.
Used as a Catalyst in Chemical Reactions:
Due to its reactive nature, 6-chloropyridine-3-sulfonic acid is also used as a catalyst to enhance the rate of chemical reactions, improving the efficiency and selectivity of various synthetic processes.

Check Digit Verification of cas no

The CAS Registry Mumber 17624-08-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,6,2 and 4 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 17624-08:
(7*1)+(6*7)+(5*6)+(4*2)+(3*4)+(2*0)+(1*8)=107
107 % 10 = 7
So 17624-08-7 is a valid CAS Registry Number.
InChI:InChI=1/C5H4ClNO3S/c6-5-2-1-4(3-7-5)11(8,9)10/h1-3H,(H,8,9,10)

17624-08-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-Chloropyridine-3-sulfonic acid

1.2 Other means of identification

Product number -
Other names 3-Pyridinesulfonicacid,6-chloro

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:17624-08-7 SDS

17624-08-7Relevant articles and documents

Preparation method of aromatic sulfonic acid compound

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Paragraph 0021, (2016/11/17)

The invention discloses a preparation method of an aromatic sulfonic acid compound, and aims to provide the preparation method of the aromatic sulfonic acid compound, wherein the method is simple in process, low in equipment requirements, high in capacity, wide in raw material sources and small in environmental influence. The method is characterized by comprising the steps: with a starting material aromatic amine compound, dissolving in an acid, carrying out a diazotization reaction with sodium nitrite to prepare a diazocompound; carrying out a reaction of a catalyst cuprous salt with a thionyl chloride aqueous solution, and carrying out a sulfonylation reaction with the prepared diazocompound to obtain an aromatic sulfonyl chloride compound or an aromatic sulfonyl chloride hydrochloride compound, next hydrolyzing to obtain a crude product aromatic sulfonic acid compound, finally purifying through a beating way by an acidic solvent and an alcohol solution, and thus obtaining the high-purity aromatic sulfonic acid compound. The method is friendly to environment, has certain cost advantages, avoids use of more expensive aromatic thiol compounds as starting materials, and is beneficial for industrial production.

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