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2,4-DIMETHOXYBENZENESULFONAMIDE, with the molecular formula C8H11NO4S, is a sulfonamide derivative characterized by the presence of two methoxy groups on the benzene ring. This chemical compound is recognized for its anti-inflammatory and anticancer properties, positioning it as a significant building block in the pharmaceutical industry for the synthesis of drugs and bioactive molecules. Its multidisciplinary applications in medicinal chemistry research, organic, and materials chemistry underscore its versatility and scientific importance.

51770-71-9

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51770-71-9 Usage

Uses

Used in Pharmaceutical Industry:
2,4-DIMETHOXYBENZENESULFONAMIDE is used as a building block for the synthesis of various drugs and bioactive molecules due to its chemical structure and pharmacological properties.
Used in Medicinal Chemistry Research:
2,4-DIMETHOXYBENZENESULFONAMIDE is used as a research compound for exploring its anti-inflammatory and anticancer properties, contributing to the development of new therapeutic agents.
Used in Organic Chemistry:
2,4-DIMETHOXYBENZENESULFONAMIDE is utilized in organic chemistry for its potential applications in the synthesis of complex organic molecules and the study of chemical reactions involving sulfonamide derivatives.
Used in Materials Chemistry:
2,4-DIMETHOXYBENZENESULFONAMIDE is employed in materials chemistry to investigate its potential use in the development of new materials with specific properties, such as those with enhanced bioactivity or stability.

Check Digit Verification of cas no

The CAS Registry Mumber 51770-71-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,7,7 and 0 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 51770-71:
(7*5)+(6*1)+(5*7)+(4*7)+(3*0)+(2*7)+(1*1)=119
119 % 10 = 9
So 51770-71-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H11NO4S/c1-12-6-3-4-8(14(9,10)11)7(5-6)13-2/h3-5H,1-2H3,(H2,9,10,11)

51770-71-9 Well-known Company Product Price

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  • Alfa Aesar

  • (H31707)  2,4-Dimethoxybenzenesulfonamide, 96%   

  • 51770-71-9

  • 1g

  • 980.0CNY

  • Detail

  • Alfa Aesar

  • (H31707)  2,4-Dimethoxybenzenesulfonamide, 96%   

  • 51770-71-9

  • 5g

  • 3273.0CNY

  • Detail

51770-71-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-Dimethoxybenzenesulfonamide

1.2 Other means of identification

Product number -
Other names 2,4-DIMETHOXYBENZENESULFONAMIDE

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:51770-71-9 SDS

51770-71-9Relevant academic research and scientific papers

Enantioselective One-pot Synthesis of 3-Azabicyclo[3.1.0]hexanes via Allylic Substitution and Oxidative Cyclization

Chaki, Bijan Mohon,Takenaka, Kazuhiro,Zhu, Linpeng,Tsujihara, Tetsuya,Takizawa, Shinobu,Sasai, Hiroaki

, p. 1537 - 1547 (2020/03/24)

An enantioselective one-pot synthesis of 3-azabicyclo[3.1.0]hexanes from allyl carbonates and propargyl amines is reported. An amine catalyst promoted the allylic substitution to form intermediary N-allyl propargylamines, which underwent enantioselective Pd(II)/Pd(IV)-mediated oxidative cyclization in situ. The chiral ligand (P,R,R)-i-Pr-SPRIX is crucial to the cyclization, producing the desired bicyclic compounds in up to 92% yield and 90% ee. (Figure presented.).

Electrochemically generatedN-iodoaminium species as key intermediates for selective methyl sulphonylimination of tertiary amines

Huang, Binbin,Yang, Chao,Zhou, Jia,Xia, Wujiong

supporting information, p. 5010 - 5013 (2020/05/18)

Reported herein is a straightforward protocol for approachingN-sulphonylamidinesviaan electricity-driven, iodine-mediated cross dehydrogenative condensation (CDC) between sulphonamides and tertiary amines, which features exclusive N-CH3selectivity for the amine partners. Mechanistic studies indicate that anin situgeneratedN-iodoaminium species serves as the key intermediate.

Monomethylthio analogues of 1-(2,4,5-trimethoxyphenyl)-2-aminopropane

Jacob III,Anderson III,Meshul,Shulgin,Castagnoli Jr.

, p. 1235 - 1239 (2007/10/06)

Regiospecific syntheses of the three monomethylthio analogues of 1-(2,4,5- trimethoxyphenyl)-2-aminopropane are described. The three isomeric amines were evaluated for potential psychotomimetic potency using the rabbit hyperthermia assay. Enantiomeric com

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