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3-Ethyl-2-fluorophenol is an organic compound characterized by the chemical formula C8H9FO. It presents as a colorless to pale yellow liquid, exhibiting a sweet, floral scent. 3-Ethyl-2-fluorophenol is soluble in alcohol and ether, and is recognized for its utility in various chemical syntheses and applications.

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  • 1243456-02-1 Structure
  • Basic information

    1. Product Name: 3-ethyl-2-fluorophenol
    2. Synonyms: 3-ethyl-2-fluorophenol
    3. CAS NO:1243456-02-1
    4. Molecular Formula: C8H9FO
    5. Molecular Weight: 140.1548632
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1243456-02-1.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-ethyl-2-fluorophenol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-ethyl-2-fluorophenol(1243456-02-1)
    11. EPA Substance Registry System: 3-ethyl-2-fluorophenol(1243456-02-1)
  • 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: 1243456-02-1(Hazardous Substances Data)

1243456-02-1 Usage

Uses

Used in Pharmaceutical Industry:
3-Ethyl-2-fluorophenol is utilized as an intermediate in the synthesis of various pharmaceuticals, contributing to the development of new drugs and medicinal compounds due to its unique chemical structure and properties.
Used in Agrochemical Industry:
In the agrochemical sector, 3-Ethyl-2-fluorophenol serves as an intermediate, playing a crucial role in the production of pesticides and other agrochemicals that are essential for crop protection and enhancement of agricultural yields.
Used in Dye Industry:
3-Ethyl-2-fluorophenol is employed in the dye industry as an intermediate for the production of dyes, which are used in a wide range of applications including textiles, plastics, and printing inks.
Used in Fragrance Industry:
3-Ethyl-2-fluorophenol is also used as a building block in the synthesis of fragrance compounds, adding to the complexity and variety of scents used in perfumes, cosmetics, and other scented products.
Used in Biotechnology and Medicine:
3-Ethyl-2-fluorophenol has been studied for its potential antimicrobial properties, indicating its value in the fields of medicine and biotechnology, particularly for the development of new antimicrobial agents to combat resistant strains of bacteria.

Check Digit Verification of cas no

The CAS Registry Mumber 1243456-02-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,3,4,5 and 6 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1243456-02:
(9*1)+(8*2)+(7*4)+(6*3)+(5*4)+(4*5)+(3*6)+(2*0)+(1*2)=131
131 % 10 = 1
So 1243456-02-1 is a valid CAS Registry Number.

1243456-02-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-ethyl-2-fluorophenol

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:1243456-02-1 SDS

1243456-02-1Upstream product

1243456-02-1Downstream Products

1243456-02-1Relevant articles and documents

Investigation of Janus Kinase (JAK) Inhibitors for Lung Delivery and the Importance of Aldehyde Oxidase Metabolism

Wellaway, Christopher R.,Baldwin, Ian R.,Bamborough, Paul,Barker, Daniel,Bartholomew, Michelle A.,Chung, Chun-Wa,Dümpelfeld, Birgit,Evans, John P.,Fazakerley, Neal J.,Homes, Paul,Keeling, Steven P.,Lewell, Xiao Q.,McNab, Finlay W.,Morley, Joanne,Needham, Deborah,Neu, Margarete,Van Oosterhout, Antoon J. M.,Pal, Anshu,Reinhard, Friedrich B. M.,Rianjongdee, Francesco,Robertson, Craig M.,Rowland, Paul,Shah, Rishi R.,Sherriff, Emma B.,Sloan, Lisa A.,Teague, Simon,Thomas, Daniel A.,Wellaway, Natalie,Wojno-Picon, Justyna,Woolven, James M.,Coe, Diane M.

, p. 633 - 664 (2022/01/03)

The Janus family of tyrosine kinases (JAK1, JAK2, JAK3, and TYK2) play an essential role in the receptor signaling of cytokines that have been implicated in the pathogenesis of severe asthma, and there is emerging interest in the development of small-molecule-inhaled JAK inhibitors as treatments. Here, we describe the optimization of a quinazoline series of JAK inhibitors and the results of mouse lung pharmacokinetic (PK) studies where only low concentrations of parent compound were observed. Subsequent investigations revealed that the low exposure was due to metabolism by aldehyde oxidase (AO), so we sought to identify quinazolines that were not metabolized by AO. We found that specific substituents at the quinazoline 2-position prevented AO metabolism and this was rationalized through computational docking studies in the AO binding site, but they compromised kinome selectivity. Results presented here highlight that AO metabolism is a potential issue in the lung.

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