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125903-39-1

4-(1H-Imidazol-2-yl)-benzoic acid methyl ester is an organic compound characterized by the chemical formula C11H10N2O2. It is a methyl ester derivative of 4-(1H-imidazol-2-yl)benzoic acid, known for its white to off-white solid appearance and solubility in organic solvents such as methanol and ethanol. The presence of the imidazole group in its structure endows it with potential for use in drug development and research, making it a significant chemical in the pharmaceutical and research fields.

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  • 125903-39-1 Structure

  • Basic information

    1. Product Name: 4-(1H-IMIDAZOL-2-YL)-BENZOIC ACID METHYL ESTER
    2. Synonyms: Benzoic acid, 4-(1H-iMidazol-2-yl)-, Methyl ester;METHYL 4-(1H-2-IMIDAZOLYL)BENZOATE;Methyl 4-(imidazol-2-yl)benzoate
    3. CAS NO:125903-39-1
    4. Molecular Formula: C11H10N2O2
    5. Molecular Weight: 202.21
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 125903-39-1.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 4-(1H-IMIDAZOL-2-YL)-BENZOIC ACID METHYL ESTER(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-(1H-IMIDAZOL-2-YL)-BENZOIC ACID METHYL ESTER(125903-39-1)
    11. EPA Substance Registry System: 4-(1H-IMIDAZOL-2-YL)-BENZOIC ACID METHYL ESTER(125903-39-1)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 125903-39-1(Hazardous Substances Data)

125903-39-1 Usage

Uses

Used in Pharmaceutical Industry:
4-(1H-Imidazol-2-yl)-benzoic acid methyl ester is used as a building block for the synthesis of various pharmaceuticals and biologically active compounds. Its imidazole group provides a versatile platform for the development of new drugs and the study of imidazole-containing compounds, which are known for their wide range of biological activities.
Used in Research Applications:
In the research field, 4-(1H-Imidazol-2-yl)-benzoic acid methyl ester serves as a valuable chemical for the investigation of imidazole-containing compounds and their potential applications. Its unique structure allows researchers to explore its properties and interactions with other molecules, contributing to the advancement of scientific knowledge and the discovery of novel therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 125903-39-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,9,0 and 3 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 125903-39:
(8*1)+(7*2)+(6*5)+(5*9)+(4*0)+(3*3)+(2*3)+(1*9)=121
121 % 10 = 1
So 125903-39-1 is a valid CAS Registry Number.

125903-39-1SDS

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 Methyl 4-(1H-imidazol-2-yl)benzoate

1.2 Other means of identification

Product number -
Other names -

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:125903-39-1 SDS

125903-39-1Relevant articles and documents

A simple and convenient one-pot method for the preparation of heteroaryl-2-imidazoles from nitriles

Voss, Matthew E.,Beer, Catherine M.,Mitchell, Scott A.,Blomgren, Peter A.,Zhichkin, Paul E.

, p. 645 - 651 (2008/04/12)

A simple, convenient and high-yielding one-pot method for the synthesis of 2-heterocycle-substituted imidazoles from the corresponding nitriles has been developed. The procedure is easily scaleable and the workup does not involve chromatography. This synthesis is also applicable to the preparation of imidazoles with electron-poor aryl substituents.

Synthesis and Cardiac Electrophysiological Activity of N-Substituted-4-(1H-imidazol-1-yl)benzamides-New Selective Class III Agents

Morgan, Thomas K.,Lis, Randall,Lumma, William C.,Nickisch, Klaus,Wohl, Ronald A.,et al.

, p. 1091 - 1097 (2007/10/02)

The synthesis and cardiac electrophysiological activity of 18 N-substituted imidazolylbenzamides or benzenesulfonamides are described.Compounds 6a,d,f-k and 11 exhibited potency in the in vitro Purkinje fiber assay comparable to that of N-2-(diethylamino

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