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2-(1H-imidazol-1-yl)isonicotinonitrile is a heterocyclic chemical compound characterized by the molecular formula C9H7N5. It features an imidazole ring fused to a pyridine ring, which endows it with unique chemical and potential pharmacological properties. 2-(1H-imidazol-1-yl)isonicotinonitrile is recognized for its role as a versatile building block in the synthesis of pharmaceuticals and other organic compounds, making it a significant entity in organic chemistry and pharmaceutical research.

158020-84-9

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158020-84-9 Usage

Uses

Used in Pharmaceutical Synthesis:
2-(1H-imidazol-1-yl)isonicotinonitrile is utilized as a key intermediate in the synthesis of various pharmaceuticals and biologically active molecules. Its presence in the molecular structure of these compounds may contribute to their therapeutic effects and pharmacological profiles.
Used in Organic Chemistry Research:
In the realm of organic chemistry, 2-(1H-imidazol-1-yl)isonicotinonitrile serves as a valuable compound for studying the properties and reactions of heterocyclic systems. Its unique structure allows for exploration into the reactivity and stability of imidazole and pyridine rings, as well as their influence on the overall chemical behavior of the molecule.
Used in Drug Design and Development:
2-(1H-imidazol-1-yl)isonicotinonitrile is employed as a precursor in drug design and development, where its chemical structure can be modified to create new drugs with specific therapeutic targets. The potential biological activity of 2-(1H-imidazol-1-yl)isonicotinonitrile, attributed to its imidazole and pyridine moieties, makes it a promising candidate for the development of novel pharmaceutical agents.
Used in Chemical Synthesis Industry:
2-(1H-imidazol-1-yl)isonicotinonitrile is used as a starting material in the chemical synthesis industry for the production of a variety of organic compounds. Its versatility in forming different chemical entities makes it an essential component in the synthesis of specialty chemicals and intermediates for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 158020-84-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,8,0,2 and 0 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 158020-84:
(8*1)+(7*5)+(6*8)+(5*0)+(4*2)+(3*0)+(2*8)+(1*4)=119
119 % 10 = 9
So 158020-84-9 is a valid CAS Registry Number.

158020-84-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-imidazol-1-ylpyridine-4-carbonitrile

1.2 Other means of identification

Product number -
Other names 2-(1H-imidazol-1-yl)pyridine-4-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:158020-84-9 SDS

158020-84-9Downstream Products

158020-84-9Relevant academic research and scientific papers

Coordination compound containing 1,10-phenanthroline-shaped N-heterocyclic carbene copper (I), and application thereof

-

Paragraph 0014, (2018/07/30)

The invention discloses a coordination compound containing 1,10-phenanthroline-shaped N-heterocyclic carbene copper (I) (as well as a coordinate compound monocrystal), and application thereof. The coordination compound containing the 1,10-phenanthroline-s

One step conversion of heteroaromatic-N-oxides to imidazolo-heteroarenes

Keith, John M.

, p. 327 - 330 (2008/04/12)

(Chemical Equation Presented) Various pyridine-, quinoline-, isoquinoline-, and pyrimidine-N-oxides were converted to their corresponding α-imidazoloheteroarenes in good yield by treatment with sulfuryl diimidazole in nonpolar solvents at elevated tempera

6-heterocyclyl pyrazolo [3,4-d]pyrimidin-4-ones and compositions and method of use thereof

-

, (2008/06/13)

Novel 6-heterocyclyl-pyrazolo[3,4-d]pyrimidin-4-ones, useful in treating cardiovascular disease, are prepared by reacting a 5-amino-1H-pyrazole-4-carboxamide with heterocyclylcarboxaldehyde or by reacting a 5-amino-1H-pyrazole-4-carbonitrile with a heterocyclylcarboxamidine, followed by diazotization and hydrolysis of the resulting 4-amino-6-heterocyclyl-pyrazolo[3,4-d]pyrimidine.

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