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3-ethyl-2-[2-(1,3-thiazol-2-yl)-1H-imidazol-1-yl]methyl-3H-imidazo[4,5-c]pyridine is a complex organic compound with a unique molecular structure, featuring an ethyl group, a thiazolyl group, an imidazolylmethyl group, and an imidazopyridine ring. The presence of these multiple functional groups and rings suggests potential biological activity, making it a compound of interest for further investigation in the field of pharmacology.

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  • 2-(1-((3-ethyl-3H-imidazo[4,5-c]pyridin-2-yl)methyl)-1H-imidazol-2-yl)thiazole

    Cas No: 438553-83-4

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  • 3H-Imidazo[4,5-c]pyridine,3-ethyl-2-[[2-(2-thiazolyl)-1H-imidazol-1-yl]methyl]-

    Cas No: 438553-83-4

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  • 438553-83-4 Structure
  • Basic information

    1. Product Name: 3-ethyl-2-{[2-(1,3-thiazol-2-yl)-1H-imidazol-1-yl]methyl}-3H-imidazo[4,5-c]pyridine
    2. Synonyms:
    3. CAS NO:438553-83-4
    4. Molecular Formula: C15H14N6S
    5. Molecular Weight: 310.3769
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 438553-83-4.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 602.695°C at 760 mmHg
    3. Flash Point: 318.299°C
    4. Appearance: N/A
    5. Density: 1.45g/cm3
    6. Vapor Pressure: 0mmHg at 25°C
    7. Refractive Index: 1.773
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 3-ethyl-2-{[2-(1,3-thiazol-2-yl)-1H-imidazol-1-yl]methyl}-3H-imidazo[4,5-c]pyridine(CAS DataBase Reference)
    11. NIST Chemistry Reference: 3-ethyl-2-{[2-(1,3-thiazol-2-yl)-1H-imidazol-1-yl]methyl}-3H-imidazo[4,5-c]pyridine(438553-83-4)
    12. EPA Substance Registry System: 3-ethyl-2-{[2-(1,3-thiazol-2-yl)-1H-imidazol-1-yl]methyl}-3H-imidazo[4,5-c]pyridine(438553-83-4)
  • 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: 438553-83-4(Hazardous Substances Data)

438553-83-4 Usage

Uses

As the specific uses of 3-ethyl-2-[2-(1,3-thiazol-2-yl)-1H-imidazol-1-yl]methyl-3H-imidazo[4,5-c]pyridine are not explicitly provided in the materials, it is not possible to list its applications or the reasons for those applications. However, given the compound's complex structure and the presence of various functional groups commonly found in pharmacologically active molecules, it can be hypothesized that it may have potential uses in the pharmaceutical industry. Further laboratory and clinical studies would be required to determine its specific properties, potential therapeutic effects, and appropriate applications.

Check Digit Verification of cas no

The CAS Registry Mumber 438553-83-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,3,8,5,5 and 3 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 438553-83:
(8*4)+(7*3)+(6*8)+(5*5)+(4*5)+(3*3)+(2*8)+(1*3)=174
174 % 10 = 4
So 438553-83-4 is a valid CAS Registry Number.

438553-83-4SDS

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 2-[1-[(3-ethylimidazo[4,5-c]pyridin-2-yl)methyl]imidazol-2-yl]-1,3-thiazole

1.2 Other means of identification

Product number -
Other names 2-(1-((3-Ethyl-3H-imidazo[4,5-c]pyridin-2-yl)methyl)-1H-imidazol-2-yl)thiazole

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:438553-83-4 SDS

438553-83-4Downstream Products

438553-83-4Relevant articles and documents

Regioselective synthesis of an imidazo[4,5-c]pyridine through selective acylation of 3,4-diaminopyridine: Synthesis of CP-885,316

Caron, Stephane,Do, Nga M.,McDermott, Ruth E.,Bahmanyar

, p. 257 - 261 (2012/12/22)

CP-885,316 (1), an imidazo[4,5-c]pyridine, 4, was prepared from 3,4-diaminopyridine (9). Two routes were demonstrated using the regioselective introduction of either an acetamide at the 3-position or a tert-butylcarbamate at the 4-position.

Benzimidazole and pyridylimidazole derivatives

-

, (2008/06/13)

This invention relates to benzimidazoles, pyridylimidazoles and related bicyclic heteroaryl compounds, all of which may be described by of Formula I The invention is particularly related to such compounds that bind with high selectivity and high affinity to the benzodiazepine site of GABAA receptors. This invention also relates to pharmaceutical compositions comprising such compounds and to the use of such compounds in treatment of certain central nervous system (CNS) diseases. Novel processes for preparing compounds of Formula I are disclosed. This invention also relates to the use of benzimidazoles, pyridylimidazoles and related bicyclic heteroaryl compounds of Formula I in combination with one or more other CNS agents to potentiate the effects of the other CNS agents. Additionally this invention relates to the use such compounds as probes for the localization of GABAA receptors in tissue sections.

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