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80459-00-3

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80459-00-3 Usage

General Description

Ethanone, 2,2-difluoro-1-(2-pyridinyl)- (9CI) is a chemical compound known for its application in various scientific studies. Often used in research laboratories for synthesis, it is characterized by a distinct structure that integrates carbon, hydrogen, nitrogen, and fluorine atoms. Although there's limited information on its physical properties or specific applications, it's safety and handling instructions are crucial to follow in experimental procedures due to the presence of fluorine, a highly reactive element. As with all chemicals, proper protective measures, adherence to safety rules, and controlled conditions are necessary when handling this compound.

Check Digit Verification of cas no

The CAS Registry Mumber 80459-00-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,4,5 and 9 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 80459-00:
(7*8)+(6*0)+(5*4)+(4*5)+(3*9)+(2*0)+(1*0)=123
123 % 10 = 3
So 80459-00-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H5F2NO/c8-7(9)6(11)5-3-1-2-4-10-5/h1-4,7H

80459-00-3SDS

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 2,2-difluoro-1-pyridin-2-ylethanone

1.2 Other means of identification

Product number -
Other names 2,2-Difluoro-1-(2-Pyridinyl)-Ethanone

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:80459-00-3 SDS

80459-00-3Downstream Products

80459-00-3Relevant articles and documents

Secondary alcohol hemiacetal formation: An in situ carbonyl activation strategy

You, Lei,Anslyn, Eric V.

supporting information; experimental part, p. 5126 - 5129 (2009/12/28)

A simple strategy was studied for the reversible nucleophilic addition of secondary alcohols to carbonyl-based receptors to form hemiacetals. It involves the in situ binding of neighboring Bronsted and Lewis acids activators. The addition reaction was suc

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