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227184-02-3

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227184-02-3 Usage

General Description

ETHYL 4-FLUORO-3-OXOPENTANOATE, also known as ethyl 4-fluoro-3-oxovalerate, is an organic compound with the molecular formula C7H11FO3. It is a clear, colorless liquid with a fruity odor. This chemical is widely used in the pharmaceutical and agrochemical industries as an intermediate in the synthesis of various compounds, including pesticides and pharmaceutical drugs. It is also used as a flavoring agent and fragrance ingredient in the production of perfumes and cosmetics. ETHYL 4-FLUORO-3-OXOPENTANOATE is considered to be a valuable building block in organic synthesis, and its properties and chemical structure make it suitable for a wide range of applications.

Check Digit Verification of cas no

The CAS Registry Mumber 227184-02-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,7,1,8 and 4 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 227184-02:
(8*2)+(7*2)+(6*7)+(5*1)+(4*8)+(3*4)+(2*0)+(1*2)=123
123 % 10 = 3
So 227184-02-3 is a valid CAS Registry Number.

227184-02-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name ETHYL 4-FLUORO-3-OXOPENTANOATE

1.2 Other means of identification

Product number -
Other names Ethyl4-fluoro-3-oxopentanoate

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:227184-02-3 SDS

227184-02-3Downstream Products

227184-02-3Relevant articles and documents

A facile synthesis of α-fluoro ketones catalyzed by [Cp*IrCl2]2

Ahlsten, Nanna,Bartoszewicz, Agnieszka,Agrawal, Santosh,Martin-Matute, Belen

supporting information; experimental part, p. 2600 - 2608 (2011/10/02)

Allylic alcohols are isomerized into enolates (enols) by [Cp*IrCl2]2. The enolates react with Selectfluor present in the reaction media. This method produces α-fluoro ketones as single constitutional isomers in high yields. Georg Thieme Verlag Stuttgart. New York.

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