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88377-32-6

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88377-32-6 Usage

Description

2-(2-CARBOXY-PHENYLAMINO)-3-METHOXY-BENZOIC ACID, also known as 2-[(2-Carboxyphenyl)amino]-3-methoxybenzoic Acid (CAS# 88377-32-6), is an organic compound with a unique chemical structure that features a carboxyphenylamino group attached to a methoxybenzoic acid backbone. 2-(2-CARBOXY-PHENYLAMINO)-3-METHOXY-BENZOIC ACID possesses versatile chemical properties, making it a valuable intermediate in various organic synthesis processes.

Uses

Used in Organic Synthesis:
2-(2-CARBOXY-PHENYLAMINO)-3-METHOXY-BENZOIC ACID is used as a synthetic intermediate for the development of various organic compounds. Its unique structure allows for the creation of a wide range of molecules with potential applications in different industries, such as pharmaceuticals, agrochemicals, and materials science.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-(2-CARBOXY-PHENYLAMINO)-3-METHOXY-BENZOIC ACID is used as a key building block for the synthesis of novel drug candidates. Its chemical versatility enables the development of new molecules with potential therapeutic properties, contributing to the discovery of innovative treatments for various diseases and conditions.
Used in Agrochemical Industry:
2-(2-CARBOXY-PHENYLAMINO)-3-METHOXY-BENZOIC ACID is also utilized in the agrochemical industry as a precursor for the synthesis of new pesticides and herbicides. Its unique structure can be modified to create compounds with enhanced efficacy and selectivity, leading to the development of more effective and environmentally friendly agricultural products.
Used in Materials Science:
In the field of materials science, 2-(2-CARBOXY-PHENYLAMINO)-3-METHOXY-BENZOIC ACID is employed as a component in the development of advanced materials with specific properties. Its incorporation into polymers, coatings, and other materials can result in improved performance characteristics, such as enhanced stability, durability, or functionality.

Check Digit Verification of cas no

The CAS Registry Mumber 88377-32-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,3,7 and 7 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 88377-32:
(7*8)+(6*8)+(5*3)+(4*7)+(3*7)+(2*3)+(1*2)=176
176 % 10 = 6
So 88377-32-6 is a valid CAS Registry Number.

88377-32-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-((2-Carboxyphenyl)amino)-3-methoxybenzoic acid

1.2 Other means of identification

Product number -
Other names 2-(2-carboxyanilino)-3-methoxybenzoic 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:88377-32-6 SDS

88377-32-6Downstream Products

88377-32-6Relevant articles and documents

DEUTERATED ANALOGS OF ELACRIDAR

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Paragraph 0028; 00180-00181, (2019/10/15)

The present invention relates to efflux inhibitor compounds, compositions, and methods of using the same. More specifically, the instant invention comprises deuterated analogs of elacridar with superior pharmacokinetic properties such that it is now possi

Synthesis and small-animal positron emission tomography evaluation of [11C]-elacridar as a radiotracer to assess the distribution of P-glycoprotein at the blood-brain barrier

D?rner, Bernd,Kuntner, Claudia,Bankstahl, Jens P.,Bankstahl, Marion,Stanek, Johann,Wanek, Thomas,Stundner, Gloria,Mairinger, Severin,L?scher, Wolfgang,Müller, Markus,Langer, Oliver,Erker, Thomas

supporting information; experimental part, p. 6073 - 6082 (2010/03/24)

With the aim to develop a positron emission tomography (PET) tracer to assess the distribution of P-glycoprotein (P-gp) at the blood-brain barrier (BBB) in vivo, the potent third-generation P-gp inhibitor elacridar (1) was labeled with 11C by r

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