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2-(2-TRIFLUOROMETHYLBENZOYL)PYRIDINE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

898779-76-5

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898779-76-5 Usage

Physical state

White solid

Structure

Aromatic, consisting of a pyridine ring fused with a benzene ring and a trifluoromethylbenzoyl group attached to the pyridine ring

Uses

Reagent and intermediate in organic synthesis, production of pharmaceuticals, agrochemicals, and other fine chemicals, building block in the synthesis of complex organic molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 898779-76-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,8,7,7 and 9 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 898779-76:
(8*8)+(7*9)+(6*8)+(5*7)+(4*7)+(3*9)+(2*7)+(1*6)=285
285 % 10 = 5
So 898779-76-5 is a valid CAS Registry Number.
InChI:InChI=1/C13H8F3NO/c14-13(15,16)10-6-2-1-5-9(10)12(18)11-7-3-4-8-17-11/h1-8H

898779-76-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name pyridin-2-yl-[2-(trifluoromethyl)phenyl]methanone

1.2 Other means of identification

Product number -
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

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:898779-76-5 SDS

898779-76-5Downstream Products

898779-76-5Relevant academic research and scientific papers

Photoinduced Divergent Alkylation/Acylation of Pyridine N-Oxides with Alkynes under Anaerobic and Aerobic Conditions

Xu, Jin-Hui,Wu, Wen-Bin,Wu, Jie

, p. 5321 - 5325 (2019)

Ortho-alkylated and ortho-acylated pyridines have been conveniently synthesized from pyridine N-oxides and alkynes under visible-light-mediation in a metal-free manner. The alkynes served as both alkylating and acylating agents via switching between anaerobic and aerobic conditions. The overall strategy accommodates a broad scope of substituted pyridine N-oxides and alkynes, with excellent regioselectivity in a number of cases.

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