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1082949-99-2

Tert-butyl 4-(2-(4-fluoro-3-(trifluoromethyl)phenyl)-2-oxoethylcarbamoyl)piperidine-1-carboxylate is a complex organic compound characterized by a piperidine ring, a common structural motif in pharmaceuticals and chemical reactions. This ring is connected to a tert-butyl carboxylate, a 4-fluoro-3-(trifluoromethyl)phenyl group, and a 2-oxoethylcarbamoyl moiety, which together contribute to a rich potential for chemical reactivity and diversity. The incorporation of multiple fluorine atoms in the molecule endows it with unique chemical properties due to the high electronegativity of fluorine. Although the specific applications are not detailed, tert-butyl 4-(2-(4-fluoro-3-(trifluoromethyl)phenyl)-2-oxoethylcarbamoyl)piperidine-1-carboxylate may find utility in synthetic chemistry, pharmaceutical development, and material chemistry.

1082949-99-2

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  • 1-Piperidinecarboxylic acid, 4-[[[2-[4-fluoro-3-(trifluoromethyl)phenyl]-2-oxoethyl]amino]carbonyl]-, 1,1-dimethylethyl ester

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  • 1-Piperidinecarboxylic acid, 4-[[[2-[4-fluoro-3-(trifluoromethyl)phenyl]-2-oxoethyl]amino]carbonyl]-, 1,1-dimethylethyl ester

    Cas No: 1082949-99-2

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  • tert-butyl 4-(2-(4-fluoro-3-(trifluoromethyl)phenyl)-2-oxoethylcarbamoyl)piperidine-1-carboxylate

    Cas No: 1082949-99-2

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1082949-99-2 Usage

Uses

Used in Synthetic Chemistry:
Tert-butyl 4-(2-(4-fluoro-3-(trifluoromethyl)phenyl)-2-oxoethylcarbamoyl)piperidine-1-carboxylate is used as a synthetic intermediate for the preparation of various complex organic molecules, leveraging its diverse functional groups and reactivity.
Used in Pharmaceutical Development:
In the pharmaceutical industry, tert-butyl 4-(2-(4-fluoro-3-(trifluoromethyl)phenyl)-2-oxoethylcarbamoyl)piperidine-1-carboxylate is used as a lead compound for the development of new drugs, potentially targeting a range of therapeutic areas due to its unique molecular structure and chemical properties.
Used in Material Chemistry:
Tert-butyl 4-(2-(4-fluoro-3-(trifluoromethyl)phenyl)-2-oxoethylcarbamoyl)piperidine-1-carboxylate is utilized as a component in the synthesis of advanced materials, where its fluorinated and carbamoyl groups may contribute to specific material properties such as stability, reactivity, or selectivity in various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 1082949-99-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,8,2,9,4 and 9 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1082949-99:
(9*1)+(8*0)+(7*8)+(6*2)+(5*9)+(4*4)+(3*9)+(2*9)+(1*9)=192
192 % 10 = 2
So 1082949-99-2 is a valid CAS Registry Number.

1082949-99-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl 4-[[2-[4-fluoro-3-(trifluoromethyl)phenyl]-2-oxoethyl]carbamoyl]piperidine-1-carboxylate

1.2 Other means of identification

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Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

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More Details:1082949-99-2 SDS

1082949-99-2Relevant articles and documents

NOVEL IMIDAZOLE AMINES AS MODULATORS OF KINASE ACTIVITY

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, (2013/03/28)

The invention provides novel imidazole amine compounds according to Formula (I) and Formula (II) their manufacture and use for the treatment of hyperproliferative diseases, such as cancer.

Rapid development and scale-up of a 1 H -4-substituted imidazole intermediate enabled by chemistry in continuous plug flow reactors

May, Scott A.,Johnson, Martin D.,Braden, Timothy M.,Calvin, Joel R.,Haeberle, Brian D.,Jines, Amy R.,Miller, Richard D.,Plocharczyk, Edward F.,Rener, Gregory A.,Richey, Rachel N.,Schmid, Christopher R.,Vaid, Radhe K.,Yu, Hannah

, p. 982 - 1002 (2012/08/27)

The development of reactions in a continuous fashion in plug flow tube reactors (PFR) offers unique advantages to the drug development and scale-up process and can also enable chemistry that would be difficult to perform via batch processing. Herein, we r

AKT AND P70 S6 KINASE INHIBITORS

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Page/Page column 62, (2010/06/11)

The present invention provides AKT and p70 S6 kinase inhibitors of the formula: The present invention also provides pharmaceutical compositions comprising compounds of Formula I, uses of compounds of Formula I and methods of using compounds of Formula I.

P70 S6 KINASE INHIBITORS

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Page/Page column 64, (2009/01/20)

The present invention provides p70 S6 kinase inhibitors of the formula: pharmaceutical formulations comprising them, and methods for their use.

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