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  • 866782-59-4 Structure
  • Basic information

    1. Product Name: 8-FLUORO-3-IODOQUINOLINE
    2. Synonyms: 8-FLUORO-3-IODOQUINOLINE;Quinoline, 8-fluoro-3-iodo-
    3. CAS NO:866782-59-4
    4. Molecular Formula: C9H5FIN
    5. Molecular Weight: 273.05
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 866782-59-4.mol
    9. Article Data: 6
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 324.4 °C at 760 mmHg
    3. Flash Point: 150 °C
    4. Appearance: /
    5. Density: 1.908 g/cm3
    6. Vapor Pressure: 0.000467mmHg at 25°C
    7. Refractive Index: 1.696
    8. Storage Temp.: Keep in dark place,Sealed in dry,Room Temperature
    9. Solubility: N/A
    10. PKA: -0.17±0.28(Predicted)
    11. CAS DataBase Reference: 8-FLUORO-3-IODOQUINOLINE(CAS DataBase Reference)
    12. NIST Chemistry Reference: 8-FLUORO-3-IODOQUINOLINE(866782-59-4)
    13. EPA Substance Registry System: 8-FLUORO-3-IODOQUINOLINE(866782-59-4)
  • 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: 866782-59-4(Hazardous Substances Data)

866782-59-4 Usage

Description

8-Fluoro-3-iodoquinoline is a chemical compound with the molecular formula C9H5FIN, belonging to the class of substituted quinoline, a heterocyclic aromatic organic compound. Its unique structure, featuring both fluorine and iodine atoms, endows it with interesting reactivity and properties, making it a valuable building block in organic synthesis and pharmaceutical research.

Uses

Used in Organic Synthesis:
8-Fluoro-3-iodoquinoline is used as a synthetic building block for creating new chemical compounds with diverse properties. Its presence in the molecular structure allows for the development of compounds with enhanced reactivity and stability.
Used in Pharmaceutical Research:
8-Fluoro-3-iodoquinoline is utilized as a pharmaceutical intermediate, contributing to the discovery and development of new drug molecules. Its unique structure and properties make it a promising candidate for the synthesis of potential therapeutic agents.
Used in Drug Discovery:
8-Fluoro-3-iodoquinoline is employed as a valuable compound in the field of drug discovery, where its versatile reactivity and properties can be harnessed to create novel drug candidates with potential therapeutic applications.

Check Digit Verification of cas no

The CAS Registry Mumber 866782-59-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,6,7,8 and 2 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 866782-59:
(8*8)+(7*6)+(6*6)+(5*7)+(4*8)+(3*2)+(2*5)+(1*9)=234
234 % 10 = 4
So 866782-59-4 is a valid CAS Registry Number.
InChI:InChI=1/C9H5FIN/c10-8-3-1-2-6-4-7(11)5-12-9(6)8/h1-5H

866782-59-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 8-FLUORO-3-IODOQUINOLINE

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:866782-59-4 SDS

866782-59-4Upstream product

866782-59-4Relevant articles and documents

Method for preparing 8-fluoroquinoline and method for preparing 3-iodo-8-fluoroquinoline

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Paragraph 0073-0084, (2018/03/26)

The invention provides a method for preparing 8-fluoroquinoline and a method for preparing 3-iodo-8-fluoroquinoline. Preparation of the 8-fluoroquinoline comprises the step of carrying out a ring-closure reaction between fluoroaniline and glycerin, and preparation of the 3-iodo-8-fluoroquinoline comprises the step of carrying out a substitution reaction among the prepared 8-fluoroquinoline, N-chlorosuccinimide and a metal iodide. The method has the characteristics that the raw materials are cheap and readily available, the cost is low, any special equipment is not needed, the various materialsare low in toxicity, safe, environmental-friendly, less in by-products and high in yield, and large-scale industrial production is easily realized.

NOVEL QUINOLINE COMPOUNDS CAPABLE OF BINDING AT THE CB2 RECEPTOR

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Page/Page column 16-17, (2008/06/13)

The present invention relates to novel quinoline derivatives such as compounds of the formula (I) which possess are capable of selectively modulating the cannabinoid 2 receptor and the use of such compounds or pharmaceutical compositions thereof in the tr

3-((HETERO)ARYLSULFONYL)-8-` (AMINOALKYL)OXY!QUINOLINES AS 5-HT6 RECEPTOR ANTAGONISTS FOR THE TREATMENT OF CNS DISORDERS

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Page/Page column 12, (2010/02/14)

The present invention relates to novel quinoline derivatives such as compounds of the formula (I): and the use of such compounds or pharmaceutical compositions thereof in the treatment of CNS and other disorders.

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