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5-Methoxybenzo[d]isothiazole-3-carboxylic acid is a chemical compound with the molecular formula C9H7NO4S. It is a derivative of benzo[d]isothiazole, featuring a methoxy group at the 5th position and a carboxylic acid group at the 3rd position. 5-Methoxybenzo[d]isothiazole-3-carboxylic acid is known for its potential biological and pharmacological activities, making it a promising candidate for the development of new drugs and materials. Its unique structure and properties have attracted interest for further research and potential industrial applications.

677304-76-6

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677304-76-6 Usage

Uses

Used in Pharmaceutical Synthesis:
5-Methoxybenzo[d]isothiazole-3-carboxylic acid is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure allows for the development of new drug candidates with potential therapeutic benefits.
Used in Organic Reactions:
As an intermediate in organic reactions, 5-Methoxybenzo[d]isothiazole-3-carboxylic acid plays a crucial role in the synthesis of various organic compounds. Its reactivity and functional groups enable the formation of diverse chemical products.
Used in Antitumor Research:
5-Methoxybenzo[d]isothiazole-3-carboxylic acid and its derivatives have been studied for their antitumor properties. They exhibit potential inhibitory effects on tumor growth and progression, making them valuable for the development of novel anticancer agents.
Used in Antimicrobial Applications:
5-Methoxybenzo[d]isothiazole-3-carboxylic acid has also shown promise in antimicrobial research, with potential applications in the development of new antimicrobial agents. Its ability to target and inhibit the growth of harmful microorganisms could contribute to the fight against antibiotic resistance.
Used in Drug Development:
The potential biological and pharmacological activities of 5-Methoxybenzo[d]isothiazole-3-carboxylic acid make it an attractive molecule for the development of new drugs. Its unique structure and properties can be harnessed to create innovative therapeutic agents with improved efficacy and safety profiles.

Check Digit Verification of cas no

The CAS Registry Mumber 677304-76-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,7,7,3,0 and 4 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 677304-76:
(8*6)+(7*7)+(6*7)+(5*3)+(4*0)+(3*4)+(2*7)+(1*6)=186
186 % 10 = 6
So 677304-76-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H7NO3S/c1-13-5-2-3-7-6(4-5)8(9(11)12)10-14-7/h2-4H,1H3,(H,11,12)

677304-76-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-methoxy-1,2-benzothiazole-3-carboxylic acid

1.2 Other means of identification

Product number -
Other names 5-methoxy-benzo[d]isothiazole-3-carboxylic 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:677304-76-6 SDS

677304-76-6Downstream Products

677304-76-6Relevant articles and documents

1 H-INDAZOLES, BENZOTHIAZOLES, 1,2-BENZOISOXAZOLES, 1,2-BENZOISOTHIAZOLES, AND CHROMONES AND PREPARATION AND USES THEREOF

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Page/Page column 71, (2010/11/27)

The present invention relates generally to the field of ligands for nicotinic acetylcholine receptors (nAChR), activation of nAChRs, and the treatment of -disease conditions associated with defective or malfunctioning nicotinic acetylcholine receptors, especially of the brain. Further, this invention relates to novel compounds (indazoles and benzothiazoles), which act as ligands for the α7 nAChR subtype, methods of preparing such compounds, compositions containing such compounds, and methods of use thereof.

Indoles, 1h-indazoles, 1,2-benzisoxazoles, 1,2-benzoisothiazoles, and preparation and uses thereof

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Page/Page column 39, (2008/06/13)

The present invention relates generally to the field of ligands for nicotinic acetylcholine receptors (nACh receptors), activation of nACh receptors, and the treatment of disease conditions associated with defective or malfunctioning nicotinic acetylcholine receptors, especially of the brain. Further, this invention relates to novel compounds (indazoles and benzothiazoles), which act as ligands for the α7 nACh receptor subtype, methods of preparing such compounds, compositions containing such compounds, and methods of use thereof.

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