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CAS

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203066-98-2

2'-Fluoro-4'-octyloxyacetophenone is a fluoro-substituted benzophenone with an octyloxy group attached to the 4' position, belonging to the class of aromatic ketones known as acetophenones. This chemical intermediate is recognized for its potent inhibitory activity against certain enzymes and is utilized in the synthesis of pharmaceuticals, agrochemicals, and aromatic compounds such as fragrances and flavors.

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  • 203066-98-2 Structure

  • Basic information

    1. Product Name: 2'-FLUORO-4'-OCTYLOXYACETOPHENONE
    2. Synonyms: 2'-FLUORO-4'-N-OCTYLOXYACETOPHENONE;2-FLUORO-4-N-OCTYLOXYACETOPHENONE;2'-FLUORO-4'-OCTYLOXYACETOPHENONE
    3. CAS NO:203066-98-2
    4. Molecular Formula: C16H23FO2
    5. Molecular Weight: 266.35
    6. EINECS: N/A
    7. Product Categories: Adehydes, Acetals & Ketones;Anisoles, Alkyloxy Compounds & Phenylacetates;Fluorine Compounds
    8. Mol File: 203066-98-2.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 357.1 °C at 760 mmHg
    3. Flash Point: 164 °C
    4. Appearance: /
    5. Density: 1.019 g/cm3
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. Water Solubility: at 25 deg C (mg/L): 0.1684
    10. CAS DataBase Reference: 2'-FLUORO-4'-OCTYLOXYACETOPHENONE(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2'-FLUORO-4'-OCTYLOXYACETOPHENONE(203066-98-2)
    12. EPA Substance Registry System: 2'-FLUORO-4'-OCTYLOXYACETOPHENONE(203066-98-2)

  • Safety Data

    1. Hazard Codes: Xi
    2. Statements: 36/37/38
    3. Safety Statements: 26-36/37/39
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 203066-98-2(Hazardous Substances Data)

203066-98-2 Usage

Uses

Used in Pharmaceutical Industry:
2'-Fluoro-4'-octyloxyacetophenone is used as a chemical intermediate for the synthesis of various pharmaceuticals, leveraging its enzyme inhibitory properties to contribute to the development of drugs for a range of medical conditions.
Used in Agrochemical Industry:
In the agrochemical sector, 2'-Fluoro-4'-octyloxyacetophenone serves as a key intermediate in the production of agrochemicals, potentially enhancing crop protection and management through its enzyme inhibitory activity.
Used in Fragrance and Flavor Industry:
2'-Fluoro-4'-octyloxyacetophenone is utilized as a component in the creation of fragrances and flavors due to its aromatic properties, adding unique scents and tastes to various consumer products.

Check Digit Verification of cas no

The CAS Registry Mumber 203066-98-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,3,0,6 and 6 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 203066-98:
(8*2)+(7*0)+(6*3)+(5*0)+(4*6)+(3*6)+(2*9)+(1*8)=102
102 % 10 = 2
So 203066-98-2 is a valid CAS Registry Number.

203066-98-2SDS

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 1-(2-fluoro-4-octoxyphenyl)ethanone

1.2 Other means of identification

Product number -
Other names 2'-Fluoro-4'-octyloxyacetophenone

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:203066-98-2 SDS

203066-98-2Relevant articles and documents

Influence of fluoro substituents on the mesophase behaviour of banana-shaped molecules

Bedel,Rouillon,Marcerou,Laguerre,Nguyen,Achard

, p. 2214 - 2220 (2007/10/03)

Three new series of bent-shaped five-ring liquid crystals, based on the ester of isophthalic acid as the central core and azomethine linkages, are presented. They differ by the number and the position of halogeno substituents on the outer rings. This lateral substitution strongly influences the type of mesophases formed. Calculations were performed to determine the modification of the distribution of charge along the different molecules.

Effects of fluoro-substitution on mesogenic properties of copper and oxovanadium(IV) complexes derived from β-(4-alkoxyphenyl)-dialdehydes

Blake,Chipperfield,Clark

, p. 305 - 308 (2007/10/03)

Fluoro-substitution in the phenyl ring of some β-(4-alkoxyphenyl)-dialdehydes markedly affects the mesophase behaviour of their copper(II) and oxovanadium(IV) complexes. Fluoro-substitution in the 2-position of the octyl and decyl copper(II) derivatives l

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