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3-(PENTAFLUOROPHENYL)PROPIONYL CHLORIDE, with the molecular formula C9H4ClF5O, is a colorless liquid characterized by a pungent odor. It is a carboxylic acid derivative and a versatile building block in organic chemistry, known for its ability to participate in various chemical reactions such as acylation, nucleophilic substitution, and esterification. 3-(PENTAFLUOROPHENYL)PROPIONYL CHLORIDE is recognized for its role as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds, contributing significantly to the production of a diverse array of chemical products across different industries.

2063-40-3

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2063-40-3 Usage

Uses

Used in Pharmaceutical Industry:
3-(PENTAFLUOROPHENYL)PROPIONYL CHLORIDE is used as a synthetic intermediate for the development of various pharmaceuticals. Its reactivity and structural properties make it suitable for creating new drug molecules, potentially leading to advancements in medicinal chemistry.
Used in Agrochemical Industry:
In the agrochemical sector, 3-(PENTAFLUOROPHENYL)PROPIONYL CHLORIDE is utilized as a key component in the synthesis of agrochemicals. Its ability to form stable derivatives is valuable for creating effective and durable products for agricultural applications.
Used in Organic Chemistry Research:
3-(PENTAFLUOROPHENYL)PROPIONYL CHLORIDE is employed as a research tool in organic chemistry. It serves as a model compound for studying reaction mechanisms and exploring new synthetic pathways, thereby contributing to the broader understanding of organic reactions.
Used in Chemical Product Manufacturing:
3-(PENTAFLUOROPHENYL)PROPIONYL CHLORIDE is used as a building block in the manufacturing of a wide range of chemical products. Its versatility in undergoing various chemical reactions allows for the creation of diverse end products used in multiple industries.
It is important to handle 3-(PENTAFLUOROPHENYL)PROPIONYL CHLORIDE with care due to its corrosive nature, which may cause skin, eye, and respiratory irritation. Proper safety measures should be taken to mitigate any potential hazards associated with its use.

Check Digit Verification of cas no

The CAS Registry Mumber 2063-40-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,6 and 3 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2063-40:
(6*2)+(5*0)+(4*6)+(3*3)+(2*4)+(1*0)=53
53 % 10 = 3
So 2063-40-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H4ClF5O/c10-4(16)2-1-3-5(11)7(13)9(15)8(14)6(3)12/h1-2H2

2063-40-3Relevant academic research and scientific papers

Treatment of mastitis

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Example 4, (2008/06/13)

The invention provides new fluorinated cephalosporin antibiotics of Formula I wherein Ra, Rb, Rc, Rdand Re, independently, are H, F or a C1-C6alkyl-(Z)n— group having at least one fluorine substituent; X is O or S; Y is S, O, or —CH2—; Z is O, S, —SO—, or —SO2—; m and n independently are 0 or 1; and R1is H, C1-C6-alkyl, phenyl or benzyl, each of which may optionally have up to three substituents selected from halo, C1-C4-alkoxy, phenyl, NO2, C1-C6-alkanoyl, benzoyl, or C1-C6-alkanoyloxy; or a physiologically acceptable salt thereof; and methods of preventing or treating or treating infection, particularly mastitis in ruminants, using these antibiotics.

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