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Quinoline-3-sulfonic acid is an organic compound with the chemical formula C9H7NO3S. It is a derivative of quinoline, a heterocyclic aromatic compound, where a sulfonic acid group (-SO3H) is attached to the 3-position of the quinoline ring. Quinoline-3-sulfonic acid is known for its acidic properties due to the presence of the sulfonic acid group, which can ionize in water to release hydrogen ions (H+). Quinoline-3-sulfonic acid is used in various applications, including as an intermediate in the synthesis of dyes and pharmaceuticals, and in analytical chemistry as a reagent. Its solubility in water and its ability to form salts make it a versatile compound in chemical research and industrial processes.

6046-41-9

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6046-41-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6046-41-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,4 and 6 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6046-41:
(6*6)+(5*0)+(4*4)+(3*6)+(2*4)+(1*1)=79
79 % 10 = 9
So 6046-41-9 is a valid CAS Registry Number.

6046-41-9SDS

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 Quinoline-3-sulfonic acid

1.2 Other means of identification

Product number -
Other names 3-quinolinesulfonic 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:6046-41-9 SDS

6046-41-9Upstream product

6046-41-9Downstream Products

6046-41-9Relevant academic research and scientific papers

Aqueous process chemistry: The preparation of aryl sulfonyl chlorides

Hogan, Philip J.,Cox, Brian G.

experimental part, p. 875 - 879 (2010/04/22)

The use of aqueous acidic conditions for the preparation of arylsulfonyl chlorides from diazonium salts in the presence of copper salts, preferably CuCl, together with thionyl chloride as the sulfur dioxide source, has considerable advantages over recommended literature procedures, whereby reactions are carried out in acetic acid with minimisation of water content of the solvent. The method has been shown to be successful for a wide range of electron-deficient and electron-neutral aryl substrates. The sulfonyl chlorides are protected from hydrolysis by their low solubility in water, which results in their direct precipitation from the reaction mixture in good yields (>70%) and high strength (>98% w/w). The aqueous process, which is additionally safer and more robust, can be readily scaled up and has significant environmental benefits.

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