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119448-82-7

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119448-82-7 Usage

Description

ETHYL 2-PHENYLIMIDAZO[1,2-A]PYRIDINE-3-CARBOXYLATE is a chemical compound characterized by the molecular formula C19H14N2O2. It features a distinctive imidazo-pyridine ring structure, which endows it with potential biological and pharmacological properties. ETHYL 2-PHENYLIMIDAZO[1,2-A]PYRIDINE-3-CARBOXYLATE is predominantly utilized in the pharmaceutical sector as a key building block for the synthesis of a variety of drugs and pharmaceutical compounds.

Uses

Used in Pharmaceutical Industry:
ETHYL 2-PHENYLIMIDAZO[1,2-A]PYRIDINE-3-CARBOXYLATE serves as a crucial intermediate in the synthesis of drugs and pharmaceutical compounds. Its unique chemical structure allows it to be a valuable component in the development of new medications for diverse therapeutic areas.
However, it is important to note that the specific applications and reasons for using ETHYL 2-PHENYLIMIDAZO[1,2-A]PYRIDINE-3-CARBOXYLATE in different industries or for particular purposes are not provided in the materials. Further research and testing are required to fully explore and understand its potential uses and effects.

Check Digit Verification of cas no

The CAS Registry Mumber 119448-82-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,4,4 and 8 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 119448-82:
(8*1)+(7*1)+(6*9)+(5*4)+(4*4)+(3*8)+(2*8)+(1*2)=147
147 % 10 = 7
So 119448-82-7 is a valid CAS Registry Number.
InChI:InChI=1/C16H14N2O2/c1-2-20-16(19)15-14(12-8-4-3-5-9-12)17-13-10-6-7-11-18(13)15/h3-11H,2H2,1H3

119448-82-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl 2-phenylimidazo[1,2-a]pyridine-3-carboxylate

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:119448-82-7 SDS

119448-82-7Relevant articles and documents

Structural Determinants for the Mode of Action of Imidazopyridine DS2 at δ-Containing γ-Aminobutyric Acid Type A Receptors

Rostrup, Frederik,Falk-Petersen, Christina B.,Harpsoe, Kasper,Buchleithner, Stine,Conforti, Irene,Jung, Sascha,Gloriam, David E.,Schirmeister, Tanja,Wellendorph, Petrine,Frolund, Bente

, p. 4730 - 4743 (2021)

Despite the therapeutic relevance of δ-containing γ-aminobutyric acid type A receptors (GABAARs) and the need for δ-selective compounds, the structural determinants for the mode and molecular site of action of δ-selective positive allosteric modulator imi

PYRAZOLE AND IMIDAZOLE DERIVATIVES, COMPOSITIONS AND METHODS AS OREXIN ANTAGONISTS

-

Page/Page column 35; 43, (2020/12/29)

The present invention is directed to substituted Pyrazole and Imidazole derivatives of compounds that are antagonists of orexin receptors, and which are useful in the treatment or prevention of neurological and psychiatric disorders and diseases in which

NBS mediated protocol for the synthesis of N-bridged fused heterocycles in water

Bhagat, Saket B.,Telvekar, Vikas N.

supporting information, p. 3662 - 3666 (2017/08/23)

A facile and environmental friendly protocol for the synthesis of N-bridged fused bicyclic compounds such as imidazo[1,2-a]pyridines, imidazo[1,2-a]pyrimidines, and imidazo[2,1-b]thiazole, from commercially available starting materials has been developed.

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