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167884-21-1

(3-ChloroiMidazo[1,2-a]pyridin-6-yl)Methanol is a chemical compound characterized by its molecular formula C9H7ClN2O. It features a chloro group, an imidazole ring, a pyridine ring, and a hydroxymethyl group. (3-ChloroiMidazo[1,2-a]pyridin-6-yl)Methanol is known for its unique structure and properties, which contribute to its reactivity and versatility in various chemical reactions.

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  • 167884-21-1 Structure

  • Basic information

    1. Product Name: (3-ChloroiMidazo[1,2-a]pyridin-6-yl)Methanol
    2. Synonyms: (3-ChloroiMidazo[1,2-a]pyridin-6-yl)Methanol;3-chloro-Imidazo[1,2-a]pyridine-6-methanol
    3. CAS NO:167884-21-1
    4. Molecular Formula: C8H7ClN2O
    5. Molecular Weight: 182.60698
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 167884-21-1.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: (3-ChloroiMidazo[1,2-a]pyridin-6-yl)Methanol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (3-ChloroiMidazo[1,2-a]pyridin-6-yl)Methanol(167884-21-1)
    11. EPA Substance Registry System: (3-ChloroiMidazo[1,2-a]pyridin-6-yl)Methanol(167884-21-1)

  • 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: 167884-21-1(Hazardous Substances Data)

167884-21-1 Usage

Uses

Used in Organic Synthesis:
(3-ChloroiMidazo[1,2-a]pyridin-6-yl)Methanol is utilized as a reagent in organic synthesis for its ability to participate in a range of chemical reactions. Its unique structure allows it to be a valuable tool in the creation of new organic compounds.
Used in Pharmaceutical Research:
In the pharmaceutical industry, (3-ChloroiMidazo[1,2-a]pyridin-6-yl)Methanol is employed as a reagent to aid in the development of new drugs and pharmaceuticals. Its potential applications in drug discovery are attributed to its distinctive structural features and reactivity, making it a promising candidate for researchers in medicinal chemistry.
Used in Drug Development:
(3-ChloroiMidazo[1,2-a]pyridin-6-yl)Methanol is used as a key intermediate in the synthesis of various drug candidates. Its unique properties and reactivity enable the development of novel therapeutic agents with potential applications in treating a wide range of medical conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 167884-21-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,7,8,8 and 4 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 167884-21:
(8*1)+(7*6)+(6*7)+(5*8)+(4*8)+(3*4)+(2*2)+(1*1)=181
181 % 10 = 1
So 167884-21-1 is a valid CAS Registry Number.

167884-21-1SDS

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 (3-chloroimidazo[1,2-a]pyridin-6-yl)methanol

1.2 Other means of identification

Product number -
Other names 3-chloro-Imidazo[1,2-a]pyridine-6-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:167884-21-1 SDS

167884-21-1Relevant articles and documents

THIOZOLIDINEDIONE DERIVATIVES AS P13 KINASE INHIBITORS

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Page/Page column 56, (2008/06/13)

Invented is a method of inhibiting the activity/function of PB kinases using thiozolidinedione derivatives. Also invented is a method of treating one or more disease states selected from: autoimmune disorders, inflammatory diseases, cardiovascular diseases, neurodegenerative diseases, allergy, asthma, pancreatitis, multiorgan failure, kidney diseases, platelet aggregation, cancer, sperm motility, transplantation rejection, graft rejection and lung injuries by the administration of thiozolidinedione derivatives.

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