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33097-39-1

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33097-39-1 Usage

General Description

3,6-difluoropyridazine is a chemical compound with the molecular formula C4H2F2N2. It is a heterocyclic aromatic organic compound that contains a six-membered ring with two nitrogen atoms and two fluorine atoms attached to adjacent carbon atoms. 3,6-difluoropyridazine is mainly used as a building block in the synthesis of various pharmaceuticals and agrochemicals. It is also utilized as a precursor in the manufacture of dyes, pigments, and other organic compounds. 3,6-difluoropyridazine is known for its high reactivity and is commonly used in organic chemistry as a versatile intermediate for the preparation of diverse chemical products. Despite its usefulness, 3,6-difluoropyridazine should be handled with care, as it is flammable and may pose health hazards if not properly managed.

Check Digit Verification of cas no

The CAS Registry Mumber 33097-39-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,0,9 and 7 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 33097-39:
(7*3)+(6*3)+(5*0)+(4*9)+(3*7)+(2*3)+(1*9)=111
111 % 10 = 1
So 33097-39-1 is a valid CAS Registry Number.
InChI:InChI=1/C4H2F2N2/c5-3-1-2-4(6)8-7-3/h1-2H

33097-39-1SDS

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 3,6-Difluoropyridazine

1.2 Other means of identification

Product number -
Other names Pyridazine,3,6-difluoro

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:33097-39-1 SDS

33097-39-1Upstream product

33097-39-1Relevant articles and documents

-

Johnson et al.

, p. 7505 (1970)

-

Room-temperature nucleophilic aromatic fluorination: Experimental and theoretical studies

Sun, Haoran,DiMagno, Stephen G.

, p. 2720 - 2725 (2007/10/03)

(Chemical Equation Presented) Taming the reagent: The use of anhydrous tetrabutylammonium fluoride (TBAFanh) in nucleophilic aromatic substitution reactions, including variants of the selective halogen-exchange and fluorodenitration processes (see scheme), was investigated. It was shown that TBAFanh permits these reactions to be performed under surprisingly mild conditions if it is used in relatively nonpolar media.

The proton sponge-triethylamine tris(hydrogen fluoride) system as a selective nucleophilic fluorinating reagent for chlorodiazines

Darabantu, Mirce,Lequeux, Thierry,Pommelet, Jean-Claude,Plé, Nelly,Turck, Alain,Toupet, Lo?c

, p. 6763 - 6767 (2007/10/03)

The proton sponge-triethylamine tris(hydrogen fluoride) mixture provides a mild and efficient fluorinating - reagent for the selective introduction of a fluorine atom, by halogen exchange, into dichlorodiazines. (C) 2000 Elsevier Science Ltd.

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