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34256-01-4

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34256-01-4 Usage

Description

3-Methoxy-benzenesulfonic acid, also known as p-anisylsulfonic acid, is a chemical compound with the molecular formula C7H8O4S. It is a member of the sulfonic acids class and is characterized by its white to pale yellow crystalline powder form, which is soluble in water and other polar solvents. This versatile and important chemical reagent is widely used in various industries, including pharmaceuticals and chemical manufacturing, as a key intermediate for the synthesis of a range of compounds.

Uses

Used in Pharmaceutical Industry:
3-Methoxy-benzenesulfonic acid is used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its ability to facilitate specific chemical transformations makes it a valuable component in the development of new drugs and medications.
Used in Chemical Industry:
In the chemical industry, 3-Methoxy-benzenesulfonic acid serves as a crucial reagent in organic synthesis, contributing to the production of a variety of chemical products. Its versatility in facilitating reactions is essential for the synthesis of complex organic molecules.
Used in Dye Manufacturing:
3-Methoxy-benzenesulfonic acid is utilized in the dye manufacturing process, where it plays a role in the synthesis of different types of dyes. Its chemical properties allow for the creation of a wide range of colorants used in various applications.
Used as a Catalyst in Chemical Reactions:
3-Methoxy-benzenesulfonic acid is employed as a catalyst to accelerate various chemical reactions. Its presence helps to increase the rate of reaction, improving the efficiency of chemical processes in industrial settings.
Used in the Production of Agrochemicals:
3-Methoxy-benzenesulfonic acid is also used in the agrochemical sector, where it aids in the synthesis of agrochemical products. Its role in facilitating specific chemical transformations is vital for the development of effective agricultural chemicals.
Used in Specialty Chemicals Manufacturing:
3-Methoxy-benzenesulfonic acid finds application in the production of specialty chemicals, where its unique properties are harnessed to create tailored chemical products for specific industries and applications.

Check Digit Verification of cas no

The CAS Registry Mumber 34256-01-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,2,5 and 6 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 34256-01:
(7*3)+(6*4)+(5*2)+(4*5)+(3*6)+(2*0)+(1*1)=94
94 % 10 = 4
So 34256-01-4 is a valid CAS Registry Number.

34256-01-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Methoxybenzenesulfonic acid

1.2 Other means of identification

Product number -
Other names 3-Methoxy-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:34256-01-4 SDS

34256-01-4Relevant articles and documents

Phenylthio-derivatives of α-methylene-γ-lactones as pro-drugs of cytotoxic agents

Fardella, Giuseppe,Barbetti, Paolo,Grandolini, Giuliano,Chiappini, Ione,Ambrogi, Valeria,Scarcia, Vito,Furlani Candiani, Ariella

, p. 515 - 523 (2007/10/03)

A series of substituted phenylthio-derivatives of grosheimin (1), a natural cytotoxic guaianolide, were investigated with the aim of providing insight into their mechanism of action as cytotoxic agents against KB cell lines. Hydrolysis data, kinetics, in the presence and in the absence of H2O2, and the valuation of lipophilicity were correlated with cytotoxicity values and with Hammett-σ-values of substituents (R) at the thiophenol ring. These compounds behave as 'pro-drugs' which release the cytotoxic agent grosheimin by sulphur-oxidation promoted by H2O2 and subsequent retro- elimination which depends on the nature and position of the R substituent.

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