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Ethyl 3-(2,6-difluorophenyl)-3-oxopropanoate, also known as ethyl 2,6-difluorophenyl glyoxylate, is a chemical compound with the molecular formula C11H11F2O3. It is a white solid at room temperature with a faint odor. ethyl 3-(2,6-difluorophenyl)-3-oxopropanoate is commonly used in organic synthesis and serves as an intermediate in the production of various pharmaceuticals and agrochemicals. It is stable under normal storage and handling conditions but can be hazardous if ingested or inhaled, necessitating careful handling and adherence to proper safety procedures.

97305-12-9

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97305-12-9 Usage

Uses

Used in Pharmaceutical Industry:
Ethyl 3-(2,6-difluorophenyl)-3-oxopropanoate is used as a chemical intermediate for the synthesis of various pharmaceuticals. Its unique structure and reactivity make it a valuable component in the development of new drugs and medications.
Used in Agrochemical Industry:
In the agrochemical industry, ethyl 3-(2,6-difluorophenyl)-3-oxopropanoate is utilized as an intermediate in the production of various agrochemicals. Its properties contribute to the creation of effective and targeted pest control solutions and other agricultural applications.
Used in Organic Synthesis:
Ethyl 3-(2,6-difluorophenyl)-3-oxopropanoate is employed as a key component in organic synthesis processes. Its versatility and reactivity allow for the creation of a wide range of organic compounds, further expanding its applications across various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 97305-12-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,3,0 and 5 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 97305-12:
(7*9)+(6*7)+(5*3)+(4*0)+(3*5)+(2*1)+(1*2)=139
139 % 10 = 9
So 97305-12-9 is a valid CAS Registry Number.

97305-12-9SDS

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 ethyl 3-(2,6-difluorophenyl)-3-oxopropanoate

1.2 Other means of identification

Product number -
Other names ethyl 2,6-difluorobenzoylacetate

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:97305-12-9 SDS

97305-12-9Relevant academic research and scientific papers

HERBICIDAL CINNOLINE DERIVATIVES

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Page/Page column 38-39, (2021/11/26)

Compounds of the Formula (I) wherein the substituents are as defined in claim 1. The invention further relates to herbicidal compositions which comprise a compound of Formula (I) and to the use of compounds of Formula (I) for controlling weeds, in particu

HERBICIDAL CINNOLINE DERIVATIVES

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Page/Page column 45, (2021/11/26)

Compounds of the formula (I), wherein the substituents are as defined in claim 1. The invention further relates to herbicidal compositions which comprise a compound of Formula (I) and to the use of compounds of Formula (I) for controlling weeds, in partic

PYRAZOLO [4,3-c] CINNOLIN-3-ONE M1 RECEPTOR POSITIVE ALLOSTERIC MODULATORS

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Page/Page column 40; 41, (2010/09/17)

The present invention is directed to pyrazolo [4,3-c] cinnolin-3-one compounds of formula (I) which are M1 receptor positive allosteric modulators and that are useful in the treatment of diseases in which the M1 receptor is involved, such as Alzheimer's disease, schizophrenia, pain or sleep disorders. The invention is also directed to pharmaceutical compositions comprising the compounds, and to the use of the compounds and compositions in the treatment of diseases mediated by the M1 receptor.

Reinvestigation of prototropic photochromism: 3-Benzoyl-2-benzylchromones

Rossollin,Lokshin,Samat,Guglielmetti

, p. 7725 - 7731 (2007/10/03)

The synthesis of a series of new nine 3-benzoyl-2-benzylchromones is developed through a classical and an optimized Kostanecki-Robinson method involving an o-hydroxyphenyl-β-diketone and an acid anhydride. The different spectrokinetic studies carried out in solution and in polymer matrixes have highlighted the main structure/photochromic parameters relationships and the influence of the medium on the photochromic properties.

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