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6-(trifluoroMethoxy)pyridin-2-aMine is a chemical compound characterized by the molecular formula C7H6F3NO. It features an aromatic amine structure with a pyridine ring that is substituted with a trifluoromethoxy group at the 6-position. 6-(trifluoroMethoxy)pyridin-2-aMine is recognized for its unique chemical and physical properties, which arise from the presence of the trifluoromethoxy group, and it plays a significant role as a building block in the synthesis of pharmaceuticals and agrochemicals, as well as a reagent in chemical reactions, particularly for the formation of carbon-carbon bonds.

1131007-45-8

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1131007-45-8 Usage

Uses

Used in Pharmaceutical and Agrochemical Industries:
6-(trifluoroMethoxy)pyridin-2-aMine is utilized as a key intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its unique properties and reactivity make it a valuable component in the development of new drugs and pesticides, contributing to advancements in healthcare and agriculture.
Used as a Reagent in Organic Chemistry:
In the field of organic chemistry, 6-(trifluoroMethoxy)pyridin-2-aMine serves as a reagent, especially in reactions that involve the formation of carbon-carbon bonds. Its presence can enhance the efficiency and selectivity of these reactions, facilitating the creation of complex organic molecules.
Used in Research and Development:
6-(trifluoroMethoxy)pyridin-2-aMine is also employed in research and development settings, where its unique properties are explored for potential applications in new technologies and materials. Its versatility and reactivity make it a promising candidate for further scientific investigation and innovation.

Check Digit Verification of cas no

The CAS Registry Mumber 1131007-45-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,3,1,0,0 and 7 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1131007-45:
(9*1)+(8*1)+(7*3)+(6*1)+(5*0)+(4*0)+(3*7)+(2*4)+(1*5)=78
78 % 10 = 8
So 1131007-45-8 is a valid CAS Registry Number.

1131007-45-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-(trifluoromethoxy)pyridin-2-amine

1.2 Other means of identification

Product number -
Other names 2-amino-6-trifluoromethoxypyridine

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:1131007-45-8 SDS

1131007-45-8Upstream product

1131007-45-8Downstream Products

1131007-45-8Relevant academic research and scientific papers

A general approach to (trifluoromethoxy)pyridines: First X-ray structure determinations and quantum chemistry studies

Manteau, Baptiste,Genix, Pierre,Brelot, Lydia,Vors, Jean-Pierre,Pazenok, Sergiy,Giornal, Florence,Leuenberger, Charlotte,Leroux, Frederic R.

experimental part, p. 6043 - 6066 (2011/02/26)

The previously unknown 2-, 3-, and 4-(trifluoromethoxy)pyridines have now become readily accessible by means of an efficient and straightforward large-scale synthesis. Their regioselective functionalization by organometallic methods has been studied and has afforded new and highly important building blocks for life-sciences-oriented research. In addition, the first X-ray crystallographic structure determinations of (trifluoromethoxy)pyridines have been performed. Lowest-energy conformations of (trifluoromethoxy)pyridines and (trifluoromethoxy)pyridinium cations were determined by in silico studies. A general and efficient route to (trifluoromethoxy)pyridines is reported. Regioselective functionalization by organometallic methods afforded new and highly important building blocks for life-sciences-oriented research. The first X-ray crystallographic structure determinations of (trifluoromethoxy)pyridines have been performed and supported by in silico studies.

METHOD FOR THE PREPARATION OF FUNCTIONALIZED TRIHALOMETHOXY SUBSTITUTED PYRIDINES

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Page/Page column 51-52, (2010/04/28)

The present invention pertains to a process for the preparation of functionalized trihalomethoxypyridines of formula (I) comprising reacting hydroxypyridines with thiophosgene in the presence of a base; reacting the obtained chlorothionoformiates with elemental chlorine and finally converting trichloromethoxy pyridines to trihalomethoxy pyridines using a fluoride source.

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