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4,6-difluoropyrimidine is a chemical compound with the molecular formula C4H2F2N2, belonging to the pyrimidine group of organic compounds. It is characterized by the presence of two fluorine atoms on the 4th and 6th positions of the pyrimidine ring structure, which endows it with unique properties and reactivity.

2802-62-2

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2802-62-2 Usage

Uses

Used in Pharmaceutical Industry:
4,6-difluoropyrimidine is used as a building block for the synthesis of various biologically active compounds due to its unique structure and reactivity. It plays a crucial role in the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical industry, 4,6-difluoropyrimidine is utilized as a key intermediate in the synthesis of agrochemicals, contributing to the development of effective pesticides and other agricultural chemicals.
Used in Material Science:
4,6-difluoropyrimidine may have applications in the field of material science, where its unique properties can be harnessed to create novel materials with specific characteristics for various applications.
Used as a Reagent in Organic Chemistry Reactions:
Due to its reactivity, 4,6-difluoropyrimidine serves as an important reagent in various organic chemistry reactions, facilitating the synthesis of a wide range of valuable substances.

Check Digit Verification of cas no

The CAS Registry Mumber 2802-62-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,0 and 2 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2802-62:
(6*2)+(5*8)+(4*0)+(3*2)+(2*6)+(1*2)=72
72 % 10 = 2
So 2802-62-2 is a valid CAS Registry Number.
InChI:InChI=1/C4H2F2N2/c5-3-1-4(6)8-2-7-3/h1-2H

2802-62-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,6-Difluoropyrimidine

1.2 Other means of identification

Product number -
Other names 4,6-DIFLUOROPYRIMIDINE

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:2802-62-2 SDS

2802-62-2Upstream product

2802-62-2Relevant academic research and scientific papers

DIARYL UREA DERIVATIVES USEFUL FOR THE TREATMENT OF PROTEIN KINASE DEPENDENT DISEASES

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Page 115, (2008/06/13)

The invention relates to the use of diaryl urea derivatives in the treatment of protein kinase dependent diseases or for the manufacture of pharmaceutical compositions for use in the treatment of said diseases, methods of use of diaryl urea derivatives in the treatment of said diseases, pharmaceutical preparations comprising diaryl urea derivatives for the treatment of said diseases, diaryl urea derivatives for use in the treatment of said diseases, novel diaryl urea derivatives, pharmaceutical preparations comprising these novel diaryl urea derivatives, processes for the manufacture of the novel diaryl urea derivatives, the use or methods of use of the novel diaryl urea derivatives as mentioned above, and/or these novel diaryl urea derivatives for use in the treatment of the animal or human body.

Process for the preparation of unsymmetrical 4,6-bis(aryloxy) pyrimidine compounds

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, (2008/06/13)

There is provided a process for the preparation of unsymmetrical 4,6-bis(aryloxy)pyrimidine compounds. The unsymmetrical 4,6-bis(aryloxy)pyrimidine compounds are useful as pesticidal agents.

Process for the preparation of unsymmertical 4,6-Bis (aryloxy pyrimidine compounds

-

, (2008/06/13)

There is provided a process for the preparation of unsymmetrical 4,6-bis(aryloxy)pyrimidine compounds. The unsymmetrical 4,6-bis(aryloxy)pyrimidine compounds are useful as pesticidal agents.

Halogen-Exchange Fluorination of Aromatic Halides with HF or HF-Base

Fukuhara, Tsuyoshi,Yoneda, Norihiko

, p. 509 - 512 (2007/10/02)

Heteroatomic halides such as 2-chloropyrimidines and 2-chloropyridines, and 2,4-dinitrochlorobenzene underwent halogen-exchange fluorination with the treatment of HF or HF-base solutions to afford the corresponding fluorides in good yields.

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