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6256-96-8

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6256-96-8 Usage

General Description

2,5,6-trifluoropyridine-3,4-diaMine is a chemical compound with the molecular formula C5H4F3N3. It is a derivative of pyridine, a six-membered ring with five carbon atoms and one nitrogen atom. The compound contains three fluorine atoms and a diamine functional group, which consists of two amino groups (-NH2) attached to the pyridine ring at positions 3 and 4. 2,5,6-trifluoropyridine-3,4-diaMine has applications in the field of organic synthesis and pharmaceutical research, where it can be used as a building block for the creation of more complex molecules. Its specific properties and uses may vary depending on the context in which it is employed.

Check Digit Verification of cas no

The CAS Registry Mumber 6256-96-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,5 and 6 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6256-96:
(6*6)+(5*2)+(4*5)+(3*6)+(2*9)+(1*6)=108
108 % 10 = 8
So 6256-96-8 is a valid CAS Registry Number.

6256-96-8SDS

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 2,5,6-trifluoropyridine-3,4-diamine

1.2 Other means of identification

Product number -
Other names 3,4-diamino-trifluoropyridine

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:6256-96-8 SDS

6256-96-8Relevant articles and documents

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.

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