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459-06-3

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459-06-3 Usage

Description

1-Fluoro-4-isopropoxybenzene is a chemical compound with the molecular formula C10H13FO. It is a colorless liquid that is insoluble in water but soluble in organic solvents. This versatile chemical features unique structural properties and functional groups, making it a valuable building block in various industries.

Uses

Used in Organic Synthesis:
1-Fluoro-4-isopropoxybenzene is used as a building block in organic synthesis for the production of various organic compounds. Its unique structure and functional groups contribute to the creation of a wide range of chemical products.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 1-Fluoro-4-isopropoxybenzene is used as a building block for the development of new drugs. Its properties make it a promising candidate for the synthesis of medicinal compounds with potential therapeutic applications.
Used in Pesticide Manufacturing:
1-Fluoro-4-isopropoxybenzene is used as a key component in the manufacturing of pesticides and other agricultural chemicals. Its incorporation into these products can enhance their effectiveness in protecting crops and controlling pests.
Used in Materials Science:
In the field of materials science, 1-Fluoro-4-isopropoxybenzene has potential applications due to its unique properties. It can be utilized in the development of new materials with specific characteristics, such as improved stability or reactivity.
Used as a Chemical Reaction Reagent:
Due to its functional groups and reactivity, 1-Fluoro-4-isopropoxybenzene can also serve as a reagent in various chemical reactions. This allows for the synthesis of new compounds and the modification of existing ones, broadening its applications across different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 459-06-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,5 and 9 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 459-06:
(5*4)+(4*5)+(3*9)+(2*0)+(1*6)=73
73 % 10 = 3
So 459-06-3 is a valid CAS Registry Number.

459-06-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-fluoro-4-propan-2-yloxybenzene

1.2 Other means of identification

Product number -
Other names 4-Isopropyloxy-fluorbenzol

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:459-06-3 SDS

459-06-3Downstream Products

459-06-3Relevant articles and documents

Fluorination of 4-alkyl-substituted phenols and aromatic ethers with fluoroxy and N-F reagents: Cesium fluoroxysulfate and N-fluoro-1,4-diazonia- bicyclo[2.2.2]octane dication salts case Dedicated to Prof. Dr. Boris ?emva in honor to his great contribution to fluorine chemistry.

Pravst, Igor,Stavber, Stojan

, p. 276 - 282 (2014/01/06)

4-Alkyl-substituted phenols and aromatic ethers were comparatively fluorinated with electrophilic fluorinating reagents such as cesium fluoroxysulfate (CFS), Selectfluor F-TEDA-BF4, and Accufluor NFTh in MeCN or MeOH. Reactions resulted in the formation of three types of products: 2-fluoro-4-alkyl-substituted corresponding compounds (5) as a result of ortho fluorination process, 4-alkyl-4-fluoro-cyclohexa-2,5- dienone compounds (6), resulting after an addition-elimination process, and 4-fluorosubstituted corresponding compounds (7) derived from ipso attack and release of the 4-alkyl group. The distribution of products depends on the bulkiness of alkyl groups at both positions and reaction media. The reaction in methanol proved more selective toward the formation of 2-fluoro derivatives. Tyramin and l-tyrozine were transformed with NFTh reagent in methanol to their fluorophenyl-substituted derivatives in good yield.

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