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2,6-difluoropyridine-3,4-diamine, also known as difluoropyridine diamine, is a chemical compound with the molecular formula C5H5F2N3. It is a building block commonly used in the pharmaceutical industry to synthesize a variety of active pharmaceutical ingredients. 2,6-difluoropyridine-3,4-diaMine is characterized by the presence of two fluorine atoms at the 2nd and 6th positions and two amine groups at the 3rd and 4th positions of the pyridine ring, which contributes to its unique chemical properties and reactivity.

60186-25-6

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60186-25-6 Usage

Uses

Used in Pharmaceutical Industry:
2,6-difluoropyridine-3,4-diamine is used as a key intermediate for the synthesis of various pharmaceutical drugs. Its unique chemical structure allows for the creation of a wide range of active ingredients that can be used to treat different medical conditions.
Used in Agrochemical Industry:
2,6-difluoropyridine-3,4-diaMine is also utilized as an intermediate in the synthesis of agrochemicals, which are chemicals used in agricultural practices to protect crops from pests and diseases, thereby ensuring a stable food supply.
Used in Organic Chemistry:
2,6-difluoropyridine-3,4-diamine is employed in the development of new organic compounds, thanks to its reactivity and the potential for forming various chemical bonds.
Used in Materials Science:
2,6-difluoropyridine-3,4-diaMine has potential applications in the field of materials science, where its unique properties may be harnessed to create new materials with specific characteristics, such as improved stability or reactivity.
Used in Drug Development:
2,6-difluoropyridine-3,4-diamine is used in the research and development of new drugs and pharmaceuticals, leveraging its chemical properties to design innovative therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 60186-25-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,1,8 and 6 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 60186-25:
(7*6)+(6*0)+(5*1)+(4*8)+(3*6)+(2*2)+(1*5)=106
106 % 10 = 6
So 60186-25-6 is a valid CAS Registry Number.

60186-25-6SDS

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 2,6-difluoropyridine-3,4-diamine

1.2 Other means of identification

Product number -
Other names 2,6-DIFLUORO-3,4-PYRIDINEDIAMINE

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:60186-25-6 SDS

60186-25-6Relevant academic research and scientific papers

Novel nucleosides and related processes, pharmaceutical compositions and methods

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Page/Page column 13; Figure 2, (2010/02/07)

The invention provides novel nucleosides and related processes, pharmaceutical compositions, and methods. The novel nucleosides are useful in a wide variety of antiviral, antineoplastic, and antibacterial applications. Preferred embodiments of the instant invention include novel 2 halogen-substituted, 3 halogen-substituted, and 2′,3′dihalogen-substituted analogues of 3-deazaadenosine, and novel 3 halogen-substituted analogues of 3-deazaguanosine. Compounds of the instant invention, including 4-Amino-6-fluoro-1-(β-D-ribofuranosyl)imidazo[4,5-c]pyridine and 6-Amino-7-bromo-1,5-dihydro-1-β-D-ribofuranosylimidazo[4,5-c]pyridin-4-one, have exhibited potent antiviral and anticancer activity in vitro. The compounds are also useful in the concomitant treatment of bacterial infections associated with viral infections such as AIDS.

Synthesis of halogen-substituted 3-deazaadenosine and 3-deazaguanosine analogues as potential antitumor/antiviral agents

Liu,Luo,Mozdziesz,Lin,Dutschman,Gullen,Cheng,Sartorelli

, p. 1975 - 2000 (2007/10/03)

Various 2-halogen-substituted analogues (38, 39, 43 and 44), 3-halogensubstituted analogues (51 and 52), and 2′,3′ -dihalogen- substituted analogues (57-60) of 3-deazaadenosine and 3-halogen-substituted analogues (61 and 62) of 3-deazaguanosine have been synthesized as potential anticancer and/or antiviral agents. Among these compounds, 3-deaza-3-bromoguanosine (62) showed significant cytotoxicity against L1210, P388, CCRF-CEM and B16F10 cell lines in vitro, producing IC50 values of 3, 7, 9 and 7μM, respectively. Several 3-deazaadenosine analogues (38, 51, 57 and 59) showed moderate to weak activity against hepatitis B virus.

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