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1-(2,3-dihydrobenzo[b][1,4]dioxin-6-yl)-2,2,2-trifluoroethanone, also known as trifluoroacetylbenzo[b]dioxin, is a synthetic organic compound with the molecular formula C10H7F3O3. It belongs to the class of ketones and is characterized by its unique structure and reactivity. This colorless liquid exhibits a strong, pungent odor and is soluble in organic solvents, making it a versatile building block or intermediate in various chemical syntheses.

122243-34-9

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122243-34-9 Usage

Uses

Used in Pharmaceutical Industry:
1-(2,3-dihydrobenzo[b][1,4]dioxin-6-yl)-2,2,2-trifluoroethanone is used as a key intermediate in the synthesis of pharmaceuticals for its potential applications in medicinal chemistry and drug discovery. Its unique structure and reactivity contribute to the development of novel therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical industry, 1-(2,3-dihydrobenzo[b][1,4]dioxin-6-yl)-2,2,2-trifluoroethanone serves as a building block in the synthesis of agrochemicals, such as pesticides and herbicides. Its chemical properties enable the creation of effective compounds for agricultural applications.
Used in Organic Synthesis:
1-(2,3-dihydrobenzo[b][1,4]dioxin-6-yl)-2,2,2-trifluoroethanone is utilized as a versatile intermediate in organic synthesis, allowing for the production of a wide range of organic compounds. Its reactivity and solubility in organic solvents facilitate various chemical reactions and the formation of desired products.
Used in Research Applications:
1-(2,3-dihydrobenzo[b][1,4]dioxin-6-yl)-2,2,2-trifluoroethanone is also employed in research settings for studying its chemical properties, reactivity, and potential applications in various fields. Researchers leverage its unique structure to explore new synthetic pathways and develop innovative compounds with specific functionalities.

Check Digit Verification of cas no

The CAS Registry Mumber 122243-34-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,2,4 and 3 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 122243-34:
(8*1)+(7*2)+(6*2)+(5*2)+(4*4)+(3*3)+(2*3)+(1*4)=79
79 % 10 = 9
So 122243-34-9 is a valid CAS Registry Number.

122243-34-9SDS

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-(2,3-Dihydro-1,4-benzodioxin-6-yl)-2,2,2-trifluoroethanone

1.2 Other means of identification

Product number -
Other names 1-(2,3-dihydrobenzo[b][1,4]dioxin-6-yl)-2,2,2-trifluoroethanone

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:122243-34-9 SDS

122243-34-9Downstream Products

122243-34-9Relevant academic research and scientific papers

Highly efficient synthesis of aryl and heteroaryl trifluoromethyl ketones via o-iodobenzoic acid (IBX)

Cheng, Huicheng,Pei, Yu,Leng, Faqiang,Li, Jingya,Liang, Apeng,Zou, Dapeng,Wu, Yangjie,Wu, Yusheng

, p. 4483 - 4486 (2013/07/26)

A two-step process for the synthesis of aryl and heteroaryl trifluoromethyl ketones from the corresponding aldehydes is described. Trifluoromethyl alcohols were prepared from aryl and heteroaryl aldehydes in excellent yields using catalytic amount of K2CO3. The trifluoromethyl alcohols were then oxidized conveniently and efficiently by o-iodoxybenzoic acid (IBX) under mild conditions to get the desired functionalized aryl and heteroaryl trifluoromethyl ketones.

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