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5-CHLORO-2,4-DIMETHOXY-BENZENESULFONYL CHLORIDE is a sulfonyl chloride derivative with the molecular formula C8H8ClNO4S. It features a chloro and two methoxy substituents on the benzene ring, making it a versatile chemical compound for various applications.

78046-28-3

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78046-28-3 Usage

Uses

Used in Organic Synthesis:
5-CHLORO-2,4-DIMETHOXY-BENZENESULFONYL CHLORIDE is used as a reagent for introducing the sulfonyl chloride group into organic molecules, which is crucial for the synthesis of various organic compounds.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 5-CHLORO-2,4-DIMETHOXY-BENZENESULFONYL CHLORIDE serves as a building block for the synthesis of drug compounds, contributing to the development of new medications.
Used in Dye Manufacturing:
5-CHLORO-2,4-DIMETHOXY-BENZENESULFONYL CHLORIDE is used as an intermediate in the manufacturing of dyes, playing a role in the production of colorants for various applications.
Used in Polymer Production:
This chemical compound is also utilized in the production of polymers, where it can influence the properties and characteristics of the resulting polymeric materials.
Used in Agrochemicals:
5-CHLORO-2,4-DIMETHOXY-BENZENESULFONYL CHLORIDE finds application in the agrochemical industry, where it may be used in the synthesis of pesticides or other agricultural chemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 78046-28-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,0,4 and 6 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 78046-28:
(7*7)+(6*8)+(5*0)+(4*4)+(3*6)+(2*2)+(1*8)=143
143 % 10 = 3
So 78046-28-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H8Cl2O4S/c1-13-6-4-7(14-2)8(3-5(6)9)15(10,11)12/h3-4H,1-2H3

78046-28-3SDS

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 5-chloro-2,4-dimethoxybenzenesulfonyl chloride

1.2 Other means of identification

Product number -
Other names 5-chloro-2,4-dimethoxybenzene-1-sulfonyl chloride

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:78046-28-3 SDS

78046-28-3Relevant academic research and scientific papers

N-substituted 2,4-dialkoxy benzenesulfonamides and pharmaceutical compositions

-

, (2008/06/13)

The invention relates to new N-substituted benzenesulfonamides, the process for their preparation and their use. The compounds according to the invention correspond to the general formula (I): STR1 in which: n and m have values from 0 to 4; R3 and R4 represent in particular a lower alkyl radical; R1 and R2 represent in particular hydrogen atoms, linear or branched alkyl groups having from 1 to 4 carbon atoms; R5 represents particularly a hydrogen atom, a halogen, the NO2, NH2, or CF3 group; R6 and R7 represent in particular a hydrogen atom, an alkyl radical of 1 to 6 carbon atoms. The invention is useful in the preparation of tranquilizing or anxiolytic medicines.

Substituted 2,4 dialkoxy benzene sulfonyl chlorides

-

, (2008/06/13)

The invention relates to trisubstituted sulfohalides, the process for their preparation and their use as intermediate products for the manufacture of novel compounds. The trisubstituted sulfohalides according to the invention correspond to the following general formula (I): STR1 in which: X is a halogen atom, particularly bromine or preferably chlorine; R3 and R4 each represent, independently of one another, a lower alkyl radical having from 1 to 4 carbon atoms, A represents hydrogen, halogen, alkoxy radicals having from 1 to 4 carbon atoms, alkylsulfonyl groups having from 1 to 4 carbon atoms, or the group NO2, or CF3. The invention is useful in the manufacture of medicaments.

Novel Polysulphur Bridged Metacyclophanes from the Iron-catalysed Reaction of Bis-(2,4-dimethoxyphenyl) Sulphide with Disulphur Dichloride. Evidence for the Cleavage of the Carbon-Sulphur Bond by Electrophilic Agents

Bottino, Francesco,Pappalardo, Sebastiano

, p. 718 - 722 (2007/10/02)

The iron-catalysed reaction of bis-(2,4-dimethoxyphenyl)sulphide (3) with disulphur dichloride (S2Cl2) in dilute chloroform solution has been investigated.Surprisingly, the reaction gives 4,6,11,13,18,20-hexamethoxy-1,2,9,16-tetrathiametacyclophane

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