34662-35-6

Basic information

• Product Name: 2-bromo-4-nitrobenzonitrile
• Synonyms: 2-bromo-4-nitrobenzonitrile
• CAS NO: 34662-35-6
• Molecular Formula: C₇H₃BrN₂O₂
• Molecular Weight: 227.01492
• EINECS: 604-604-1
• Mol File: 34662-35-6.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 363.301 °C at 760 mmHg
• Flash Point: 173.519 °C
• Appearance: /
• Density: 1.812 g/cm³
• CAS DataBase Reference: 2-bromo-4-nitrobenzonitrile(CAS DataBase Reference)
• NIST Chemistry Reference: 2-bromo-4-nitrobenzonitrile(34662-35-6)
• EPA Substance Registry System: 2-bromo-4-nitrobenzonitrile(34662-35-6)

Safety Data

• Hazardous Substances Data: 34662-35-6(Hazardous Substances Data)

Usage

General Description

2-Bromo-4-nitrobenzonitrile is a chemical compound used in the synthesis of various pharmaceuticals and agrochemicals. It is a yellow solid with a molecular formula C7H3BrN2O2 and a molecular weight of 219.02 g/mol. 2-Bromo-4-nitrobenzonitrile is primarily used as an intermediate in the production of several drugs and also as a building block in organic synthesis. It is classified as a nitrile, which is a functional group containing a carbon-nitrogen triple bond, and the presence of bromine and nitro groups in the compound gives it unique reactivity and properties that are valuable in the pharmaceutical and chemical industries. Due to its potential for use in the production of a variety of important compounds, 2-Bromo-4-nitrobenzonitrile is an important chemical in the field of organic synthesis.

Upstream product

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Downstream Products

• 53312-82-6 4-amino-2-bromobenzonitrile 
• 1006899-23-5 4-amino-2-cyclopropylbenzonitrile 
• 92163-95-6 2-(benzylsulfanyl)-4-nitrobenzoic acid 

Relevant articles and documents

BIARYLMETHYL HETEROCYCLES

The present invention provides compounds of Formula (I): wherein all variables are as defined in the specification, and compositions comprising any of such novel compounds. These compounds are biased agonists, or β-Arrestin agonists of the angiotensin II receptor, which may be used as medicaments.

Concise synthesis of highly substituted benzo[a]quinolizines by a multicomponent reaction/allylation/heck reaction sequence

The combination of the recently developed multicomponent construction of highly substituted 3,4-dihydropyridones with subsequent allylation and intramolecular Heck-type cyclization allows the straightforward construction of benzo[a]quinolizines, a class of polycyclic compounds that- despite their interesting pharmacological and photochemical properties- have little precedent in the literature. After optimization of the individual steps, we used this reliable three-step sequence to generate a small library of diversely substituted benzo[a]quinolizines and various heterocyclic analogs. Copyright

ISOQUINOLINE DERIVATIVES AND METHODS OF USE THEREOF

The present invention relates to Isoquinoline Derivatives, compositions comprising an effective amount of a Isoquinoline Derivative and methods for treating or preventing an inflammatory disease, a reperfusion injury, an ischemic condition, renal failure, diabetes, a diabetic complication, a vascular disease other than a cardiovascular disease, cardiovascular disease, reoxygenation injury resulting from organ transplantation, Parkinson's disease, or cancer, comprising administering to an animal in need thereof an effective amount of a Isoquinoline Derivative.