Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C5H4BrN |
| Molecular Weight | 157.996 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
BrC1=CC=CN=C1
InChI
InChIKey=NYPYPOZNGOXYSU-UHFFFAOYSA-N
InChI=1S/C5H4BrN/c6-5-2-1-3-7-4-5/h1-4H
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Synthesis of (+/-)-methyl-(1-aryl-4-pyridin-3-yl-but-3-enyl)-amines. | 2001 Dec |
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| An improved protocol for the preparation of 3-pyridyl- and some arylboronic acids. | 2002 Jul 26 |
|
| Rate-determining cooperative effects of bimolecular reactions in solution. | 2006 Dec 14 |
|
| The fate of platinum(II) and platinum(IV) anti-cancer agents in cancer cells and tumours. | 2006 Jul |
|
| Synthesis of Novel 3-Aryl-N-Methyl-1,2,5,6-Tetrahydropyridine Derivatives by Suzuki coupling: As Acetyl Cholinesterase Inhibitors. | 2007 Sep 5 |
|
| Synthetic mimic of antimicrobial peptide with nonmembrane-disrupting antibacterial properties. | 2008 Nov |
|
| Structure-activity relationships of heteroaromatic esters as human rhinovirus 3C protease inhibitors. | 2009 Jul 1 |
|
| Synthesis and crossover reaction of TEMPO containing block copolymer via ROMP. | 2010 Jun 1 |
Patents
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Code | English |
| Code System | Code | Type | Description | ||
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DTXSID9060819
Created by
admin on Fri Dec 15 18:51:30 GMT 2023 , Edited by admin on Fri Dec 15 18:51:30 GMT 2023
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210-952-0
Created by
admin on Fri Dec 15 18:51:30 GMT 2023 , Edited by admin on Fri Dec 15 18:51:30 GMT 2023
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626-55-1
Created by
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12286
Created by
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51575
Created by
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XMN8H2XE9H
Created by
admin on Fri Dec 15 18:51:30 GMT 2023 , Edited by admin on Fri Dec 15 18:51:30 GMT 2023
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3-Bromopyridine
Created by
admin on Fri Dec 15 18:51:30 GMT 2023 , Edited by admin on Fri Dec 15 18:51:30 GMT 2023
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3974
Created by
admin on Fri Dec 15 18:51:30 GMT 2023 , Edited by admin on Fri Dec 15 18:51:30 GMT 2023
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SUBSTANCE RECORD
