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4-Methoxy-3-methyl-benzenesulfonyl chloride, with the chemical formula C9H11ClO3S, is a sulfonyl chloride derivative of 4-methoxy-3-methylbenzenesulfonic acid. It is a colorless to pale yellow solid with a pungent odor and is highly reactive. 4-METHOXY-3-METHYL-BENZENESULFONYL CHLORIDE is an important intermediate in the production of pharmaceuticals, agrochemicals, and other fine chemicals. It is also used as a protecting group in organic synthesis and as a building block for various biologically-active molecules, making it a versatile and valuable chemical in the field of synthetic organic chemistry.

84910-98-5

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84910-98-5 Usage

Uses

Used in Organic Synthesis:
4-Methoxy-3-methyl-benzenesulfonyl chloride is used as a reagent for introducing the sulfonyl group into various organic molecules. Its high reactivity allows for the formation of a wide range of sulfonyl-containing compounds, which are useful in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4-Methoxy-3-methyl-benzenesulfonyl chloride is used as an intermediate in the synthesis of various drugs. Its ability to introduce the sulfonyl group into organic molecules makes it a valuable building block for the development of new pharmaceutical compounds with potential therapeutic applications.
Used in Agrochemical Industry:
4-Methoxy-3-methyl-benzenesulfonyl chloride is also used in the agrochemical industry as a key intermediate in the synthesis of various agrochemicals. The sulfonyl group introduced by 4-METHOXY-3-METHYL-BENZENESULFONYL CHLORIDE can enhance the biological activity and selectivity of agrochemicals, making them more effective in controlling pests and diseases in agriculture.
Used as a Protecting Group in Organic Synthesis:
In organic synthesis, 4-Methoxy-3-methyl-benzenesulfonyl chloride serves as a protecting group for functional groups, such as alcohols and amines. It can be easily introduced and removed during the synthesis process, allowing chemists to control the reactivity and selectivity of specific functional groups in complex organic molecules.
Used as a Building Block for Biologically-Active Molecules:
4-Methoxy-3-methyl-benzenesulfonyl chloride is used as a building block for the synthesis of various biologically-active molecules. Its sulfonyl group can be incorporated into the structure of these molecules, potentially enhancing their biological activity and providing new avenues for the development of therapeutic agents and other bioactive compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 84910-98-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,9,1 and 0 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 84910-98:
(7*8)+(6*4)+(5*9)+(4*1)+(3*0)+(2*9)+(1*8)=155
155 % 10 = 5
So 84910-98-5 is a valid CAS Registry Number.

84910-98-5SDS

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 4-methoxy-3-methylbenzenesulfonyl chloride

1.2 Other means of identification

Product number -
Other names 2-Methoxy-toluol-sulfonsaeure-(5)-chlorid

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:84910-98-5 SDS

84910-98-5Upstream product

84910-98-5Relevant academic research and scientific papers

Derivatives of 4-hydroxyphenylsulfone

-

, (2008/06/13)

4-Hydroxydiphenylsulfone derivatives represented by formula (I) wherein, R1, R2, R3 and R4, independently from one another, each denote a hydrogen atom, an alkyl group, a substituted or unsubstituted phenyl group or a cycloalkyl group, provided at least one of R1, R2, R3 and R4 is other than a hydrogen atom, and, R denotes an alkyl group, an alkenyl group, a substituted or unsubstituted phenyl group, a substituted or unsubstituted cycloalkyl group or a substituted or unsubstituted phenylalkyl group. Said compounds are useful as a developer in a heat sensitive color formation layer of a heat sensitive recording material.

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