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CasNo： 5098-11-3
Purity： 99%

We supply high quality 5-Amino-1H-imidazol-4-carbonitrile (CAS 5098-11-3), in stock, factory directly supply to clients, lower prices, more competitiveness.

What is the 4(5)-Amino-5(4)-Cyanoimidazole ?

4(5)-Amino-5(4)-Cyanoimidazole is off-white to pale yellow solid, while it's Molecular Formula is C4H4N4.

What is the CAS number for 4(5)-Amino-5(4)-Cyanoimidazole ?

The CAS number of 5-Amino-1H-imidazol-4-carbonitrile is 5098-11-3.

More information of 5-Amino-1H-imidazol-4-carbonitrile 5098-11-3 are:

Synonyms	Imidazole-4(or5)-carbonitrile, 5(or 4)-amino- (7CI);Imidazole-4-carbonitrile, 5-amino-(8CI);4-Amino-1H-imidazole-5-carbonitrile;4-Amino-5-cyanoimidazole;4-Aminoimidazole-5-carbonitrile;5-Amino-1H-imidazole-4-carbonitrile;5-Amino-4-cyanoimidazole;5-Amino-4-imidazolecarbonitrile;NSC 139091;
CAS Number	5098-11-3
Molecular Formula	C4H4N4
Molecular Weight	108.103
Density	1.42 g/cm³
Melting Point	131 °C
Boiling Point	557.7 °C at 760 mmHg
Flash Point	291.1 °C
HS CODE	2933290090
PSA	78.49000
LogP	0.44478
Pka	9.79±0.10(Predicted)

What is 4(5)-Amino-5(4)-Cyanoimidazole (5098-11-3) used for?

Compounds containing the imidazole ring, like 4(5)-amino-5(4)-cyanoimidazole, often exhibit pharmacological properties. Researchers might be exploring its potential as a drug candidate for various conditions. Imidazole derivatives have been investigated for their antimicrobial, antiviral, anticancer, and other therapeutic activities.

InChI:InChI=1/C4H4N4/c5-1-3-4(6)8-2-7-3/h2H,6H2,(H,7,8)

Articles related to 5-Amino-1H-imidazol-4-carbonitrile:

Article

Abstract

Synthesis of new substituted 5-amino-1H-imidazole-4-carbonitriles

SA Chumachenko, OV Shablykin, EB Rusanov

Russian Journal of General Chemistry, Volume 87, pages 2481–2485, (2017)

A series of new 5-amino-1H-imidazole-4-carbonitriles were synthesized based on substituted 3,3-di-amino-2-methylideneaminoprop-2-enenitriles.

Exploratory Studies to Investigate a Linked Prebiotic Origin of RNA and Coded Peptides. 3rd Communication

Karl Ace, John D. Sutherland

Chemistry & biodiversity, Volume1, Issue11 November 2004

… to 44, 45, and 46 (Fig.), but given the key role of 18 in the synthesis of the free purine nucleobases (Scheme 2), we elected to synthesise the 5-amino-1H-imidazole-4-carbonitrile Derivatives…