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2,3-Dimethoxy-5-sulphamoylbenzoic acid is a chemical compound characterized by the molecular formula C11H13NO6S. It is a benzoic acid derivative featuring two methoxy groups and a sulphonyl group attached to the benzene ring. 2,3-Dimethoxy-5-sulphamoylbenzoic acid holds potential in the pharmaceutical industry due to its structural resemblance to sulphonamide drugs, which are recognized for their antibacterial and antifungal properties. Its sulfonamide functional group also positions it as a promising candidate for medicinal chemistry and organic synthesis, where it can serve as a building block for more complex chemical compounds.

66644-80-2

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66644-80-2 Usage

Uses

Used in Pharmaceutical Industry:
2,3-Dimethoxy-5-sulphamoylbenzoic acid is used as a potential active pharmaceutical ingredient for its structural similarity to sulphonamide drugs, which are known for their antibacterial and antifungal properties. Its unique structure may contribute to the development of new drugs with enhanced efficacy and selectivity against various pathogens.
Used in Organic Synthesis:
In the field of organic synthesis, 2,3-Dimethoxy-5-sulphamoylbenzoic acid is used as a building block for the synthesis of more complex chemical compounds. Its versatile functional groups allow for various chemical reactions, enabling the creation of a wide range of molecules with potential applications in different industries.
Used in Medicinal Chemistry:
2,3-Dimethoxy-5-sulphamoylbenzoic acid is used as a starting material in medicinal chemistry for the design and synthesis of new drugs. Its sulfonamide functional group can be further modified or used as a scaffold to develop novel therapeutic agents with improved pharmacological properties.
Further research and testing on the properties and potential uses of 2,3-Dimethoxy-5-sulphamoylbenzoic acid are necessary to fully explore its capabilities and applications in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 66644-80-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,6,4 and 4 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 66644-80:
(7*6)+(6*6)+(5*6)+(4*4)+(3*4)+(2*8)+(1*0)=152
152 % 10 = 2
So 66644-80-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H11NO6S/c1-15-7-4-5(17(10,13)14)3-6(9(11)12)8(7)16-2/h3-4H,1-2H3,(H,11,12)(H2,10,13,14)

66644-80-2SDS

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-(Aminosulfonyl)-2,3-dimethoxybenzoic Acid

1.2 Other means of identification

Product number -
Other names 2,3-dimethoxy-5-sulfamoylbenzoic 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:66644-80-2 SDS

66644-80-2Downstream Products

66644-80-2Relevant academic research and scientific papers

Novel preparation method of 2,3-dimethoxy-5-sulfonamide benzoic acid

-

, (2020/05/01)

The invention discloses a novel preparation method of 2,3-dimethoxy-5-sulfonamide benzoic acid, which relates to a preparation method of a medical intermediate. The method sequentially comprises the following steps: taking 3, 4-dihydroxybenzenesulfonamide as a raw material; performing bromination and substitution reactions in sequence; and finally, carrying out hydrolysis twice to obtain the product 2,3-dimethoxy-5-sulfonamide benzoic acid. The invention provides a brand-new synthetic route, the used raw materials are wide and sufficient in source, low in price, mild in reaction condition andsimple in process, the reaction of each step is conventionally operated, the use of highly toxic dimethyl sulfate and other harmful raw materials is avoided, the pollution is reduced, and the method has a relatively good application range.

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