5-Bromonicotinonitrile
[CAS# 35590-37-5]

Identification

• Classification: Pharmaceutical intermediate >> Heterocyclic compound intermediate >> Pyridine compound >> Pyridine derivative
• Name: 5-Bromonicotinonitrile
• Synonyms: 5-Bromo-3-cyanopyridine; 5-Bromopyridine-3-carbonitrile
• Molecular Formula: C₆H₃BrN₂
• Molecular Weight: 183.00
• CAS Registry Number: 35590-37-5
• EC Number: 625-836-9
• SMILES: C1=C(C=NC=C1Br)C#N

Properties

• Density: 1.7±0.1 g/cm³ Calc.^*
• Melting point: 103 - 107 ºC (Expl.)
• Boiling point: 228.8±20.0 ºC 760 mmHg (Calc.)^*
• Flash point: 92.2±21.8 ºC (Calc.)^*
• Index of refraction: 1.612 (Calc.)^*

^* Calculated using Advanced Chemistry Development (ACD/Labs) Software.

Safety Data

• Hazard Symbols: GHS07 Warning
• Hazard Statements: H302-H312-H315-H319-H332-H335
• Precautionary Statements: P261-P264-P264+P265-P270-P271-P280-P301+P317-P302+P352-P304+P340-P305+P351+P338-P317-P319-P321-P330-P332+P317-P337+P317-P362+P364-P403+P233-P405-P501

Hazard Classification

Hazard	Class	Category Code	Hazard Statement
Skin irritation	Skin Irrit.	2	H315
Eye irritation	Eye Irrit.	2	H319
Specific target organ toxicity - single exposure	STOT SE	3	H335
Acute toxicity	Acute Tox.	4	H312
Acute toxicity	Acute Tox.	4	H302
Acute toxicity	Acute Tox.	4	H332
Acute toxicity	Acute Tox.	3	H331
Eye irritation	Eye Irrit.	2A	H319
Acute toxicity	Acute Tox.	3	H301
Acute toxicity	Acute Tox.	3	H311

Discovory and Applicatios

5-Bromonicotinonitrile is an organic compound that belongs to the class of halogenated pyridine derivatives. It consists of a pyridine ring, a nitrile group (–C≡N) at the 2-position, and a bromine atom at the 5-position on the pyridine ring. The molecular structure of 5-bromonicotinonitrile combines the characteristics of both a nitrile group and a halogen-substituted aromatic ring, making it an important intermediate for various chemical syntheses.

This compound is particularly useful in the synthesis of other organic molecules, including bioactive compounds. The nitrile group, a key functional group, is often employed in reactions that form carbon-carbon bonds and can be easily converted into other functional groups, such as amides, acids, or alcohols. The bromine atom, positioned at the 5-position of the pyridine ring, makes the compound reactive in several important organic reactions, particularly in nucleophilic substitution reactions and cross-coupling reactions. This makes 5-bromonicotinonitrile a useful intermediate in the synthesis of more complex organic molecules, including pharmaceuticals and agrochemicals.

5-Bromonicotinonitrile has been explored in the development of compounds with potential biological activity. Pyridine and nitrile-containing compounds, in general, exhibit a wide range of biological effects, such as antimicrobial, anticancer, and anti-inflammatory activities. The presence of the bromine atom further enhances the reactivity and versatility of the compound, allowing for the introduction of additional functional groups or the creation of novel molecular frameworks with potential therapeutic properties.

Additionally, 5-bromonicotinonitrile is used in materials science and as a building block for the synthesis of specialized ligands in coordination chemistry. It can also be employed in the preparation of conducting polymers and other materials with electronic properties.

In summary, 5-bromonicotinonitrile is a versatile halogenated pyridine derivative with a nitrile functional group that makes it useful in a variety of organic syntheses. It is an important intermediate in the preparation of pharmaceuticals, agrochemicals, and materials, and its bromine atom provides reactivity that enables its use in a range of chemical reactions. The compound's potential biological activity and its role in synthetic chemistry highlight its importance in both academic and industrial research.

References

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DOI: 10.1038/nchem.590

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DOI: 10.1007/s11030-017-9736-9

2013. Convenient Synthesis of Benzoxazolone Derivatives by Cross-Coupling of Benzoxazolone Boronates with Aryl Halides. Synthesis, 45(22).
DOI: 10.1055/s-0033-1339799