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3-Cyano-4,6-diaminopyridine (CDAP) is a chemical compound with the molecular formula C7H7N5, belonging to the pyridine family. It features two amino groups and a cyano group, which contribute to its unique structure and reactivity. This versatile building block is utilized in the synthesis of pharmaceuticals, agrochemicals, organic materials, and coordination polymers, making it a valuable asset in the fields of medicine, agriculture, and materials science. Furthermore, CDAP's potential antitumor and antiviral properties have garnered attention for its use in research and development.

75776-47-5

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75776-47-5 Usage

Uses

Used in Pharmaceutical Synthesis:
3-Cyano-4,6-diaminopyridine is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to form diverse chemical compounds with potential therapeutic applications.
Used in Agrochemical Development:
In the agrochemical industry, 3-Cyano-4,6-diaminopyridine is used as a precursor in the development of new agrochemicals, contributing to the creation of effective products for agricultural use.
Used in Organic Materials and Coordination Polymers:
3-Cyano-4,6-diaminopyridine is utilized as a building block in the production of organic materials and coordination polymers, owing to its unique structure that facilitates the formation of complex molecular architectures.
Used in Antitumor Research:
3-Cyano-4,6-diaminopyridine is studied as a potential antitumor agent, with ongoing research exploring its effects on tumor growth and progression, as well as its potential synergistic effects with conventional chemotherapeutic drugs.
Used in Antiviral Research:
In antiviral applications, 3-Cyano-4,6-diaminopyridine is investigated for its potential to inhibit viral replication and activity, offering a new avenue for the development of antiviral treatments.

Check Digit Verification of cas no

The CAS Registry Mumber 75776-47-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,7,7 and 6 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 75776-47:
(7*7)+(6*5)+(5*7)+(4*7)+(3*6)+(2*4)+(1*7)=175
175 % 10 = 5
So 75776-47-5 is a valid CAS Registry Number.
InChI:InChI=1/C6H6N4/c7-2-4-3-10-6(9)1-5(4)8/h1,3H,(H4,8,9,10)

75776-47-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,6-Diaminonicotinonitrile

1.2 Other means of identification

Product number -
Other names 4,6-diaminopyridine-3-carbonitrile

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:75776-47-5 SDS

75776-47-5Relevant academic research and scientific papers

Naphthyridinones for inhibiting protein tyrosine kinase and cell cycle kinase mediated cellular proliferation

-

, (2008/06/13)

PCT No. PCT/US98/16848 Sec. 371 Date Jan. 26, 2000 Sec. 102(e) Date Jan. 26, 2000 PCT Filed Aug. 13, 1998 PCT Pub. No. WO99/09030 PCT Pub. Date Feb. 25, 1999This invention relates to the inhibition of protein tyrosine kinase (PTK) and cell cycle kinase mediated cellular proliferation. More specifically, this invention relates to naphthyridinones and their use in inhibiting cellular proliferation and PTK or cell cycle kinase enzymatic activity.

A One-step Synthesis of 2,4-Bis(sec-alkylamino)-6-halo-3-pyridinecarbonitriles

Metzger, Roland,Oberdoerfer, Juergen,Schwager, Carlos,Thielecke, Wilfried,Boldt, Peter

, p. 946 - 953 (2007/10/02)

The title compounds, e.g. 2a-c or 7, are obtained by reaction of malononitrile (1) with sec-alkylhalides/aluminium chloride (except the alkyl fluorides) at room temperature.From these the corresponding 2,4-bis(sec-alkylamino)pyridines may be conveniently prepared.With hydrogen bromide, 1 or its "dimer" 10 (R = H) 2,4-diamino-6-bromo-5-pyridinecarbonitrile (17) is formed.

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