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1082951-17-4

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1082951-17-4 Usage

Description

2-aMino-1-(4-fluoro-3-(trifluoroMethyl)phenyl)ethanone 4-Methylbenzenesulfonate is a chemical compound that consists of an amino ketone and a methylbenzenesulfonate group. The amino ketone portion features a fluorine-substituted phenyl ring with a trifluoromethyl group attached to it. 2-aMino-1-(4-fluoro-3-(trifluoroMethyl)phenyl)ethanone 4-Methylbenzenesulfonate may have potential applications in the synthesis of pharmaceuticals, agrochemicals, or other organic compounds due to the presence of the amino and ketone functional groups. The 4-methylbenzenesulfonate group acts as a counterion to the positively charged amino group, contributing to the compound's stability in solid-state form and enhancing its solubility in organic solvents. As a result, 2-aMino-1-(4-fluoro-3-(trifluoroMethyl)phenyl)ethanone 4-Methylbenzenesulfonate may be utilized in research and development for various industrial and commercial purposes.

Uses

Used in Pharmaceutical Synthesis:
2-aMino-1-(4-fluoro-3-(trifluoroMethyl)phenyl)ethanone 4-Methylbenzenesulfonate is used as a synthetic intermediate for the development of pharmaceuticals, leveraging its unique structure and functional groups to create novel drug candidates.
Used in Agrochemical Production:
In the agrochemical industry, 2-aMino-1-(4-fluoro-3-(trifluoroMethyl)phenyl)ethanone 4-Methylbenzenesulfonate is used as a building block for the synthesis of new agrochemicals, potentially leading to the discovery of innovative and effective products for agricultural applications.
Used in Organic Compounds Synthesis:
2-aMino-1-(4-fluoro-3-(trifluoroMethyl)phenyl)ethanone 4-Methylbenzenesulfonate is utilized as a key component in the synthesis of various organic compounds, contributing to the advancement of organic chemistry and the development of new materials and molecules with diverse applications.

Check Digit Verification of cas no

The CAS Registry Mumber 1082951-17-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,8,2,9,5 and 1 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1082951-17:
(9*1)+(8*0)+(7*8)+(6*2)+(5*9)+(4*5)+(3*1)+(2*1)+(1*7)=154
154 % 10 = 4
So 1082951-17-4 is a valid CAS Registry Number.
InChI:InChI=1S/C16H15F4NO4S/c1-10-2-5-12(6-3-10)26(23,24)25-15(22,9-21)11-4-7-14(17)13(8-11)16(18,19)20/h2-8,22H,9,21H2,1H3

1082951-17-4SDS

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 (2-amino-1-(4-fluoro, 3-trifluoromethyl-phenyl)-ethanone) p-toluenesulfonate

1.2 Other means of identification

Product number -
Other names 2-Amino-1-(4-fluoro-3-(trifluoromethyl)phenyl)ethanone 4-methylbenzenesulfonate

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:1082951-17-4 SDS

1082951-17-4Relevant articles and documents

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

experimental part, 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

P70 S6 KINASE INHIBITORS

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Page/Page column 63-64, (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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