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213772-79-3

1-(3-FLUORO-2-IODO-QUINOLIN-4-YL)-ETHANOL is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 213772-79-3 Structure

  • Basic information

    1. Product Name: 1-(3-FLUORO-2-IODO-QUINOLIN-4-YL)-ETHANOL
    2. Synonyms: 1-(3-FLUORO-2-IODO-QUINOLIN-4-YL)-ETHANOL
    3. CAS NO:213772-79-3
    4. Molecular Formula: C11H9FINO
    5. Molecular Weight: 317.1
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 213772-79-3.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: 1-(3-FLUORO-2-IODO-QUINOLIN-4-YL)-ETHANOL(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(3-FLUORO-2-IODO-QUINOLIN-4-YL)-ETHANOL(213772-79-3)
    11. EPA Substance Registry System: 1-(3-FLUORO-2-IODO-QUINOLIN-4-YL)-ETHANOL(213772-79-3)

  • 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: 213772-79-3(Hazardous Substances Data)

213772-79-3 Usage

Chemical class

Quinolinyl ethanol

Structural features

Fluorinated and iodinated derivative of quinoline

Quinoline

Heterocyclic aromatic organic compound

Potential applications

Medicinal chemistry

Quinoline and ethanolic moieties

Useful in the development of new pharmaceutical agents

Fluorine and iodine substituents

Impart unique properties and reactivity

Pharmaceutical industry

Potential candidate for further research and development
These properties highlight the unique characteristics of 1-(3-Fluoro-2-iodo-quinolin-4-yl)-ethanol, which make it a promising compound for exploration in the field of medicinal chemistry and pharmaceutical development.

Check Digit Verification of cas no

The CAS Registry Mumber 213772-79-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,3,7,7 and 2 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 213772-79:
(8*2)+(7*1)+(6*3)+(5*7)+(4*7)+(3*2)+(2*7)+(1*9)=133
133 % 10 = 3
So 213772-79-3 is a valid CAS Registry Number.

213772-79-3SDS

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 1-(3-fluoro-2-iodoquinolin-4-yl)ethanol

1.2 Other means of identification

Product number -
Other names 4-Quinolinemethanol,3-fluoro-2-iodo-a-methyl

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:213772-79-3 SDS

213772-79-3Downstream Products

213772-79-3Relevant articles and documents

First halogen-dance reaction in quinoline series: Application to a new synthesis of quindoline

Arzel, Erwan,Rocca, Patrick,Marsais, Francis,Godard, Alain,Quéguiner, Guy

, p. 6465 - 6466 (1998)

The first halogen-dance reaction in quinoline series is described as well as a new convergent synthesis of quindoline, a natural benzo-δ- carboline.

New synthesis of benzo-δ-carbolines, cryptolepines, and their salts: In vitro cytotoxic, antiplasmodial, and antitrypanosomal activities of δ-carbolines, benzo-δ-carbolines, and cryptolepines

Arzel,Rocca,Grellier,Labae?d,Frappier,Guéritte,Gaspard,Marsais,Godard,Quéguiner

, p. 949 - 960 (2007/10/03)

The paper describes, in its first part, a new synthesis of benzo-δ-carbolines, cryptolepines, and their salts. The strategy is based on the association between halogen-dance and hetero-ring cross-coupling. It is fully convergent and regioselective with in

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