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3,3-difluorobutanoic acid, with the chemical formula C4H6F2O2, is a carboxylic acid characterized by its colorless liquid form, slightly sweet odor, and solubility in water. It has a molecular weight of 130.08 g/mol and is recognized as an important intermediate in the chemical industry.

2366-61-2

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2366-61-2 Usage

Uses

Used in Pharmaceutical Synthesis:
3,3-difluorobutanoic acid is utilized as a key intermediate for the synthesis of various pharmaceuticals, contributing to the development of new drugs and improving the efficacy of existing medications.
Used in Agrochemical Production:
3,3-difluorobutanoic acid also serves as a crucial component in the production of agrochemicals, playing a significant role in the creation of pesticides and other agricultural products to enhance crop protection and yield.
Used as a Reagent in Organic Synthesis:
3,3-difluorobutanoic acid is employed as a reagent in organic synthesis, facilitating various chemical reactions and contributing to the synthesis of complex organic compounds for diverse applications.
Used in Chemical Compound Production:
As an important intermediate, 3,3-difluorobutanoic acid is integral to the manufacturing process of a wide range of chemical compounds, highlighting its versatility and value across different sectors of the chemical industry.

Check Digit Verification of cas no

The CAS Registry Mumber 2366-61-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,6 and 6 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2366-61:
(6*2)+(5*3)+(4*6)+(3*6)+(2*6)+(1*1)=82
82 % 10 = 2
So 2366-61-2 is a valid CAS Registry Number.

2366-61-2Downstream Products

2366-61-2Relevant academic research and scientific papers

Semi-Industrial Fluorination of β-Keto Esters with SF 4: Safety vs Efficacy

Bugera, Maksym Y.,Khairulin, Andrii R.,Kliukovskyi, Denys V.,Ryabukhin, Sergey V.,Semenov, Sergey V.,Shevchenko, Valerii O.,Tarasenko, Karen V.,Trofymchuk, Serhii A.,Volochnyuk, Dmitriy M.

, p. 565 - 574 (2020/03/27)

The possibility of deoxofluorination of β-keto esters using SF 4 was investigated. The scope and limitation of the reaction were determined. The efficient method for the synthesis of β,β-difluorocarboxylic acids was elaborated based on the reaction. The set of mentioned acids, being the perspective building blocks for medicinal chemistry, were synthesized on multigram scale. The safety of SF 4 use was discussed. The described method does not improve upon the safety of using SF 4, but practical recommendations for working with the reagent are proposed. Despite the hazards of using toxic SF 4, a significant increase of efficacy in the synthesis of medicinal-chemistry-relevant building blocks, based on the reaction, in comparison with earlier described approaches is shown.

SERINE/THREONINE KINASE INHIBITORS

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Paragraph 00188, (2015/07/16)

Compounds of Formula I or a stereoisomer, tautomer or pharmaceutically acceptable salt thereof are provided, which are useful for the treatment of diseases. Methods of using compounds of Formula I or a stereoisomer, tautomer or pharmaceutically acceptable salt thereof, for in vitro, in situ, and in vivo diagnosis, prevention or treatment of such diseases, or associated pathological conditions are disclosed.

REACTION OF KETOCARBOXYLIC ESTERS WITH SULFUR TETRAFLUORIDE IN ANHYDROUS HYDROGEN FLUORIDE

Bloshchitsa, F. A.,Burmakov, A. I.,Kunshenko, B. V.,Alekseeva, L. A.,Bel'ferman, A. L.,et al.

, p. 1260 - 1263 (2007/10/02)

The reaction of ketocarboxylic esters with sulfur tetrafluoride in anhydrous hydrogen fluoride at 20 deg C gives good yields of difluorocarboxylic esters.Hydrolysis of the latter gave the corresponding carboxylic acids.

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