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2-(aminomethyl)-4-(trifluoromethyl)aniline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

765297-88-9

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765297-88-9 Usage

Appearance

White solid at room temperature

Solubility

Soluble in organic solvents

Structure

Derivative of aniline with an amino group (-NH2) and a trifluoromethyl group (-CF3) attached to the benzene ring

Usage

Commonly used as an intermediate in the production of various pharmaceuticals and agrochemicals

Industrial applications

Potential for use in organic synthesis and due to its reactivity

Biological activity

May have biological activity that warrants further investigation and research

Pharmacological properties

May have pharmacological properties that warrant further investigation and research

Check Digit Verification of cas no

The CAS Registry Mumber 765297-88-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,6,5,2,9 and 7 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 765297-88:
(8*7)+(7*6)+(6*5)+(5*2)+(4*9)+(3*7)+(2*8)+(1*8)=219
219 % 10 = 9
So 765297-88-9 is a valid CAS Registry Number.

765297-88-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(Aminomethyl)-4-(trifluoromethyl)aniline

1.2 Other means of identification

Product number -
Other names Fmoc-O1Pen-OH

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:765297-88-9 SDS

765297-88-9Relevant academic research and scientific papers

Design of a novel class of biphenyl CETP inhibitors

Lu, Zhijian,Napolitano, Joann B.,Theberge, Ashleigh,Ali, Amjad,Hammond, Milton L.,Tan, Eugene,Tong, Xinchun,Xu, Suoyu S.,Latham, Melanie J.,Peterson, Laurence B.,Anderson, Matt S.,Eveland, Suzanne S.,Guo, Qiu,Hyland, Sheryl A.,Milot, Denise P.,Chen, Ying,Sparrow, Carl P.,Wright, Samuel D.,Sinclair, Peter J.

scheme or table, p. 7469 - 7472 (2011/01/12)

A new class of CETP inhibitors was designed and prepared. These compounds are potent both in vitro and in vivo. The most active compound (12d) has shown an ability to raise HDL significantly in transgenic mouse PD model.

CETP INHIBITORS

-

Page/Page column 44-45, (2010/02/14)

Compounds of Formula (I), including pharmaceutically acceptable salts of the compounds, are CETP inhibitors, and are useful for raising HDL-cholesterol, reducing LDL-cholesterol, and for treating or preventing atherosclerosis. In the compounds of Formu

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