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2,4,6-Cycloheptatrien-1-one,2-fluoro-6-(1-methylethyl)-(9CI) is a chemical compound with the molecular formula C10H9FO. It is a fluorinated derivative of the cyclic ketone cycloheptatrienone, and its structure consists of a seven-membered ring with a fluorine atom and an isopropyl group attached to it. 2,4,6-Cycloheptatrien-1-one,2-fluoro-6-(1-methylethyl)-(9CI) is known for its unique structural and electronic properties, which make it a valuable building block in various organic synthesis reactions.

162084-58-4

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162084-58-4 Usage

Uses

Used in Organic Synthesis:
2,4,6-Cycloheptatrien-1-one,2-fluoro-6-(1-methylethyl)-(9CI) is used as a building block for the production of other fluorinated compounds. Its unique structure allows it to be a key component in the synthesis of various organic molecules, making it an essential tool in the field of organic chemistry.
Used in Pharmaceutical Industry:
2,4,6-Cycloheptatrien-1-one,2-fluoro-6-(1-methylethyl)-(9CI) is used as an intermediate in the synthesis of pharmaceutical compounds. Its fluorinated nature and structural properties contribute to the development of new drugs with improved efficacy and selectivity.
Used in Agrochemical Industry:
2,4,6-Cycloheptatrien-1-one,2-fluoro-6-(1-methylethyl)-(9CI) is used as a starting material in the production of agrochemicals. Its unique properties can be harnessed to create new pesticides or herbicides with enhanced performance and reduced environmental impact.
Used in Material Science:
2,4,6-Cycloheptatrien-1-one,2-fluoro-6-(1-methylethyl)-(9CI) is used as a component in the development of new materials. Its electronic properties and structural characteristics can be utilized to create advanced materials with improved properties, such as higher strength, better thermal stability, or enhanced electrical conductivity.
Used in Academic Research:
2,4,6-Cycloheptatrien-1-one,2-fluoro-6-(1-methylethyl)-(9CI) is used as a research compound in various scientific studies. Its unique properties make it an interesting subject for exploration in the fields of chemistry, materials science, and related disciplines, contributing to the advancement of knowledge and the development of new technologies.

Check Digit Verification of cas no

The CAS Registry Mumber 162084-58-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,2,0,8 and 4 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 162084-58:
(8*1)+(7*6)+(6*2)+(5*0)+(4*8)+(3*4)+(2*5)+(1*8)=124
124 % 10 = 4
So 162084-58-4 is a valid CAS Registry Number.

162084-58-4Upstream product

162084-58-4Downstream Products

162084-58-4Relevant academic research and scientific papers

TROPOLONE DERIVATIVES AND TAUTOMERS THEREOF FOR IRON REGULATION IN ANIMALS

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Page/Page column 170; 171, (2021/04/23)

Disclosed are a series of compounds or their tautomers having a general structure represented by Formula (la), (lb), (Ila), (lIb), or (lIc) and pharmaceutically acceptable salts thereof. The present disclosure also relates to pharmaceutical compositions comprising said compounds or tautomers. The present disclosure further relates to a method of treating a disease or condition associated with iron dysregulation or dysfunctional iron homeostasis comprising administering to a subject in need thereof a therapeutically effective amount of Formula (la), (lb), (Ila), (lIb), or (lIc) compounds or tautomers.

Conformational effects in the biological activity of fluorinated analogs of &β-thujaplicin

Murata, Kouichi,Kitazume, Tomoya

, p. 129 - 132 (2007/10/02)

Fluorination of β-thujaplicin with diethylaminosulfur trifluoride (DAST) gave 2-fluoro-4-isopropyltropone and 2-fluoro-6-isopropyltropone (1:1 mixture; 60percent).The relationships between the antibacterial activities and conformations of β-thujaplicin and its fluorinated analogs are discussed. - Keywords: Conformational effects; Biological activity; β-Thujaplicin; Fluorination; NMR spectroscopy; Semi-empirical MO calculations

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