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4-amino-2-methoxybenzamide, also known as 2-methoxy-4-amidinobenzoic acid, is a chemical compound with the molecular formula C8H10N2O3. It is a derivative of salicylamide and is commonly used in the synthesis of pharmaceuticals. This versatile chemical exhibits antiviral and antibacterial properties, making it an important component in the development of new drugs. Furthermore, it has been studied for its potential role in treating gastrointestinal disorders and as an inhibitor of various enzymes, contributing to its value in pharmaceutical research and development.

75955-30-5

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75955-30-5 Usage

Uses

Used in Pharmaceutical Synthesis:
4-amino-2-methoxybenzamide is used as a key intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of new drugs with diverse therapeutic applications.
Used in Antiviral and Antibacterial Applications:
In the medical field, 4-amino-2-methoxybenzamide is used as an antiviral and antibacterial agent due to its inherent properties that help combat viral and bacterial infections.
Used in Gastrointestinal Disorder Treatment:
4-amino-2-methoxybenzamide is utilized as a potential treatment for gastrointestinal disorders, leveraging its capacity to address specific conditions and improve patient outcomes.
Used as an Enzyme Inhibitor:
In the realm of biochemistry and pharmacology, 4-amino-2-methoxybenzamide serves as an enzyme inhibitor, playing a crucial role in modulating enzymatic activities for therapeutic benefits.
These applications highlight the multifaceted utility of 4-amino-2-methoxybenzamide in various industries, particularly in pharmaceuticals, where its unique properties are harnessed to advance treatment options and improve health outcomes.

Check Digit Verification of cas no

The CAS Registry Mumber 75955-30-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,9,5 and 5 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 75955-30:
(7*7)+(6*5)+(5*9)+(4*5)+(3*5)+(2*3)+(1*0)=165
165 % 10 = 5
So 75955-30-5 is a valid CAS Registry Number.

75955-30-5SDS

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-amino-2-methoxybenzamide

1.2 Other means of identification

Product number -
Other names 4-Amino-2-methoxy-benzoesaeure-amid

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:75955-30-5 SDS

75955-30-5Relevant academic research and scientific papers

SUBSTITUTED OXOPYRIDINE DERIVATIVES

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Paragraph 0539-0542, (2017/11/07)

The invention relates to substituted oxopyridine derivatives and to processes for preparation thereof, and also to the use thereof for production of medicaments for treatment and/or prophylaxis of diseases, especially of cardiovascular disorders, preferably thrombotic or thromboembolic disorders, and oedemas, and also ophthalmic disorders.

TANK-BINDING KINASE INHIBITOR COMPOUNDS

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Paragraph 0259, (2016/05/02)

Compounds having the following formula (I) and methods of their use and preparation are disclosed:

Oligophenylenaminones as scaffolds for α-helix mimicry

Adler, Marc J.,Hamilton, Andrew D.

experimental part, p. 7040 - 7047 (2011/10/08)

The design and synthesis of small molecule α-helix mimetics has been a productive field over the past decade. These compounds have performed well in a variety of biological systems as functional disruptors of α-helix- mediated protein-protein interactions. In our studies we have continued to develop novel, more biologically compatible scaffolds, which are often easier to assemble and capable of mimicking longer and/or more diverse helices. To this end, we have constructed a new series of i, i+4, i+7 α-helix mimics based on the enaminone scaffold. These molecules represent a step forward in the pursuit of idealized monofacial α-helix mimetics.

BENZAMIDE DERIVATIVES

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, (2010/02/10)

A compound represented by formula (1): wherein X is a single bond or a substituted or unsubstituted lower alkylene group; Z is a saturated or unsaturated monocyclic hydrocarbon ring group or the like; and each of R1, R2, R3 and R4, which may be the same or different, is a hydrogen atom, a halogen atom, a nitro group, a cyano group, a carboxyl group, a substituted or unsubstituted alkyl group, or the like, a prodrug of said compound, or a pharmaceutically acceptable salt of said compound or prodrug has inhibitory effect on Rho kinase and hence is useful for treating diseases which are such that morbidity due to them is expected to be improved by inhibition of Rho kinase and secondary effects such as inhibition of the Na+/H+ exchange transport system caused by the Rho kinase inhibition, for example, hypertension.

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