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(1H-IMIDAZOL-4-YL)(PYRIDIN-4-YL)METHANOL, commonly known as imidazopyridine, is a unique chemical compound characterized by the presence of both an imidazole and a pyridine ring in its molecular structure. This distinctive feature endows it with a wide range of biological activities, making it a promising candidate in pharmaceutical research and drug development.

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  • 185798-86-1 Structure
  • Basic information

    1. Product Name: (1H-IMIDAZOL-4-YL)(PYRIDIN-4-YL)METHANOL
    2. Synonyms: (1H-IMIDAZOL-4-YL)(PYRIDIN-4-YL)METHANOL
    3. CAS NO:185798-86-1
    4. Molecular Formula: C9H9N3O
    5. Molecular Weight: 175.19
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 185798-86-1.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: (1H-IMIDAZOL-4-YL)(PYRIDIN-4-YL)METHANOL(CAS DataBase Reference)
    10. NIST Chemistry Reference: (1H-IMIDAZOL-4-YL)(PYRIDIN-4-YL)METHANOL(185798-86-1)
    11. EPA Substance Registry System: (1H-IMIDAZOL-4-YL)(PYRIDIN-4-YL)METHANOL(185798-86-1)
  • 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: 185798-86-1(Hazardous Substances Data)

185798-86-1 Usage

Uses

Used in Pharmaceutical Research:
(1H-IMIDAZOL-4-YL)(PYRIDIN-4-YL)METHANOL is utilized as a potential drug candidate in pharmaceutical research due to its diverse biological activities and unique molecular structure. It has been studied for its potential as an antitumor, anti-inflammatory, and antiviral agent, as well as for its neurological and central nervous system modulatory properties.
Used in Drug Discovery:
In the field of drug discovery, (1H-IMIDAZOL-4-YL)(PYRIDIN-4-YL)METHANOL serves as a valuable target for medicinal chemistry studies. Its unique structure and diverse biological activities make it an attractive compound for the development of new therapeutic agents to address various health conditions and diseases.

Check Digit Verification of cas no

The CAS Registry Mumber 185798-86-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,5,7,9 and 8 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 185798-86:
(8*1)+(7*8)+(6*5)+(5*7)+(4*9)+(3*8)+(2*8)+(1*6)=211
211 % 10 = 1
So 185798-86-1 is a valid CAS Registry Number.

185798-86-1SDS

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 1H-imidazol-5-yl(pyridin-4-yl)methanol

1.2 Other means of identification

Product number -
Other names 4-Pyridinemethanol,a-1H-imidazol-5-yl

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:185798-86-1 SDS

185798-86-1Downstream Products

185798-86-1Relevant articles and documents

Unconventional acceptor and donor functional groups linked by a captodative spacer

Alcalde, Ermitas,Gisbert, Maria,Pons, Josep M.,Perez-Garcia, Lluisa

, p. 15197 - 15208 (2007/10/03)

The chemical stability to oxidation of a set of compounds built up from acceptor and donor subunits linked by a methylene or a hydroxymethylene group was studied. Whereas 1-butyl-3-[1,2,4-triazol-5(3)-ylmethyl]pyridinium salts 2d,e showed high stability to oxidation, 1-butyl-4-[imidazol-4(5)-ylhidroxymethyl]pyridinium salt 14f was oxidised spontaneously to the corresponding carbonyl compound, indicating the capability of the oxidation phenomenon to be controlled by the nature of the building blocks.

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