168072-17-1

Basic information

• Product Name: 4-BROMO-2'-CYANOBIPHENYL
• Synonyms: 4-BROMO-2'-CYANOBIPHENYL
• CAS NO: 168072-17-1
• Molecular Formula: C13H8BrN
• Molecular Weight: 258.11
• Product Categories: pharmacetical
• Mol File: 168072-17-1.mol
• Article Data: 7

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4-BROMO-2'-CYANOBIPHENYL(CAS DataBase Reference)
• NIST Chemistry Reference: 4-BROMO-2'-CYANOBIPHENYL(168072-17-1)
• EPA Substance Registry System: 4-BROMO-2'-CYANOBIPHENYL(168072-17-1)

Safety Data

• Hazardous Substances Data: 168072-17-1(Hazardous Substances Data)

Usage

General Description

4-Bromo-2'-cyanobiphenyl is a chemical compound with the molecular formula C13H8BrN. It is a brominated cyanobiphenyl, which is a type of organic compound with a biphenyl backbone and a functional group containing both bromine and cyanide. This chemical is used in organic synthesis and as a building block for the production of various materials and compounds. It is also known for its potential use in liquid crystal displays, pharmaceuticals, and other industrial applications. However, it is important to handle 4-bromo-2'-cyanobiphenyl with caution, as it may pose health and environmental risks due to its toxicity and potential for environmental persistence.

Upstream product

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• 106-37-6 1.4-dibromobenzene 
• 57598-33-1 2-(2-methoxyphenyl)-4,4-dimethyl-2-oxazoline 
• 84392-29-0 2-(4'-bromobiphenyl-2-yl)-4,4-dimethyloxazoline 
• 105901-12-0 2-(4-bromophenyl)benzamide 
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Downstream Products

• 3096-56-8 2-bromofluoren-9-one 
• 1026513-05-2 2-Butyl-6-chloro-3-{chloro-[2'-(1-trityl-1H-tetrazol-5-yl)-biphenyl-4-yl]-methyl}-4,5-dimethyl-pyridine 
• 1026534-39-3 (2-Butyl-6-chloro-4,5-dimethyl-pyridin-3-yl)-[2'-(1-trityl-1H-tetrazol-5-yl)-biphenyl-4-yl]-methanol 
• 153806-48-5 2-butyl-6-chloro-4-methyl-3-<<2'-(triphenylmethyltetrazol-5-yl)biphenyl-4-yl>hydroxymethyl>pyridine 
• 153806-49-6 2-butyl-6-chloro-4-methyl-3-<<2'-(triphenylmethyltetrazol-5-yl)biphenyl-4-yl>chloromethyl>pyridine 
• 1027315-18-9 (2-Butyl-4,5-dimethyl-pyridin-3-yl)-[2'-(1-trityl-1H-tetrazol-5-yl)-biphenyl-4-yl]-methanol 
• 1026736-63-9 2-Butyl-3-{chloro-[2'-(1-trityl-1H-tetrazol-5-yl)-biphenyl-4-yl]-methyl}-4,5-dimethyl-pyridine 
• 1025933-49-6 2-Butyl-3-{chloro-[2'-(1-trityl-1H-tetrazol-5-yl)-biphenyl-4-yl]-methyl}-4-methyl-pyridine 
• 1027414-09-0 (2-Butyl-4-methyl-pyridin-3-yl)-[2'-(1-trityl-1H-tetrazol-5-yl)-biphenyl-4-yl]-methanol 
• 1027371-83-0 2-Butyl-6-chloro-4,5-dimethyl-3-[2'-(1-trityl-1H-tetrazol-5-yl)-biphenyl-4-ylmethyl]-pyridine 
• 1027412-56-1 2-Butyl-6-chloro-4-methyl-3-[2'-(1-trityl-1H-tetrazol-5-yl)-biphenyl-4-ylmethyl]-pyridine 
• 1027030-59-6 2-Butyl-4,5-dimethyl-3-[2'-(1-trityl-1H-tetrazol-5-yl)-biphenyl-4-ylmethyl]-pyridine 
• 1026073-11-9 2-Butyl-4-methyl-3-[2'-(1-trityl-1H-tetrazol-5-yl)-biphenyl-4-ylmethyl]-pyridine 
• 139964-26-4 5-(4'-Bromo-biphenyl-2-yl)-1-trityl-1H-tetrazole 

Relevant articles and documents

ORGANIC LIGHT-EMITTING DIODE MATERIALS

Described herin are molecules for use in organic light emitting diodes. Example molecules comprise at least one acceptor moiety A, at least one donor moiety D, and optionally one or more bridge moieties B. Each moiety A is covalently attached to either the moiety B or the moeity D, each moiety D is covalently attached to either the moeity B or the moeity A, and each B is covalently attached to at least one moiety A and at least one moiety D. Values and preferred values of moieties A, D and B are defined herein.

Novel syntheses of fluorenones via nitrile-directed palladium-catalyzed C-H and dual C-H bond activation

Novel procedures for the [Pd]/[Ag]/TFA system catalyzed cascade reactions of nitrile directed remote C-H and dual C-H bond activation with insertion of nitrile were developed, which afforded variously polysubstituted fluorenones in moderate to good yields with tolerance of a wide variety of substrates.

PYRROLE AND PYRAZOLE DERIVATIVES AS POTENTIATORS OF GLUTAMATE RECEPTORS

The present invention relates to pyrrole and pyrazole compounds of formula (I) and their pharmaceutically acceptable salts, and further relates to their use in treating schizophrenia, cognitive deficits associated with schizophrenia, Alzheimer's disease, dementia of the Alzheimer's type, mild cognitive impairment, or depression. The compounds act as potentiators on glutamate receptors, in particular AMPA and the GluR family.