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6-Chloroimidazolo[1,2-A]Pyridin-2-Yl)Methanol is a chemical compound characterized by the molecular formula C8H6ClN3O. It is a white to off-white solid with a chloro group and an imidazole ring in its structure, making it a versatile building block for the synthesis of various biologically active compounds. The methanol functional group further enhances its solubility in different solvents, contributing to its potential applications in the pharmaceutical industry.

1039416-36-8

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1039416-36-8 Usage

Uses

Used in Pharmaceutical Industry:
6-Chloroimidazolo[1,2-A]Pyridin-2-Yl)Methanol is used as a pharmaceutical intermediate for the synthesis of various pharmaceuticals. Its unique structure with a chloro group and an imidazole ring allows for the development of new drugs and medication formulations.
Used in Drug Development:
6-Chloroimidazolo[1,2-A]Pyridin-2-Yl)Methanol is used as a key component in the development of new drugs due to its potential biological activity. Its presence in the molecular structure can contribute to the therapeutic effects of the final drug product.
Used in Medication Formulations:
6-Chloroimidazolo[1,2-A]Pyridin-2-Yl)Methanol is used as an ingredient in medication formulations to enhance their efficacy and solubility. The methanol functional group allows for better dissolution in various solvents, improving the overall performance of the medication.
However, it is important to note that further research and testing are necessary to fully evaluate the potential uses and properties of 6-Chloroimidazolo[1,2-A]Pyridin-2-Yl)Methanol in the pharmaceutical industry.

Check Digit Verification of cas no

The CAS Registry Mumber 1039416-36-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,9,4,1 and 6 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1039416-36:
(9*1)+(8*0)+(7*3)+(6*9)+(5*4)+(4*1)+(3*6)+(2*3)+(1*6)=138
138 % 10 = 8
So 1039416-36-8 is a valid CAS Registry Number.

1039416-36-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (6-Chloroimidazo[1,2-a]pyridin-2-yl)methanol

1.2 Other means of identification

Product number -
Other names {6-chloroimidazo[1,2-a]pyridin-2-yl}methanol

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:1039416-36-8 SDS

1039416-36-8Relevant academic research and scientific papers

Discovery of imidazopyridine derivatives as highly potent respiratory syncytial virus fusion inhibitors

Feng, Song,Hong, Di,Wang, Baoxia,Zheng, Xiufang,Miao, Kun,Wang, Lisha,Yun, Hongying,Gao, Lu,Zhao, Shuhai,Shen, Hong C.

supporting information, p. 359 - 362 (2015/03/30)

A series of imidazolepyridine derivatives were designed and synthesized according to the established docking studies. The imidazopyridine derivatives were found to have good potency and physical-chemical properties. Several highly potent compounds such as 8ji, 8jl, and 8jm were identified with single nanomolar activities. The most potent compound 8jm showed an IC50 of 3 nM, lower microsome clearance and no CYP inhibition. The profile of 8jm appeared to be superior to BMS433771, and supported further optimization.

CHEMICAL COMPOUNDS 635 : PYRIDOPYRIMIDINEDIONES AS PDE4 INHIBITORS

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Page/Page column 40-41, (2008/12/07)

The present invention provides a compound of a formula (I): wherein the variables are defined herein; to a process for preparing such a compound; and to the use of such a compound in the treatment of a PDE 4 mediated disease state.

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