2-Bromo-5-hydroxybenzonitrile

2-Bromo-5-hydroxybenzonitrile Suppliers list
Company Name: J & K SCIENTIFIC LTD.  
Tel: 18210857532 18210857532
Email: jkinfo@jkchemical.com
Company Name: Meryer (Shanghai) Chemical Technology Co., Ltd.  
Tel: 4006356688 18621169109
Email: market03@meryer.com
Company Name: ShangHai DEMO Chemical Co.,Ltd  
Tel: 400-021-7337 2355568890
Email: sales@demochem.com
Company Name: Capot Chemical Co., Ltd  
Tel: +86 (0) 571 85 58 67 18
Email:
Company Name: Shanghai Hanhong Scientific Co.,Ltd.  
Tel: 021-54306202 13764082696
Email: info@hanhongsci.com

2-Bromo-5-hydroxybenzonitrile manufacturers

2-Bromo-5-hydroxybenzonitrile Basic information
Product Name:2-Bromo-5-hydroxybenzonitrile
Synonyms:2-BroMo-5-hydroxybenzonitrle;Benzonitrile, 2-bromo-5-hydroxy-
CAS:189680-06-6
MF:C7H4BrNO
MW:198.02
EINECS:
Product Categories:Aromatic Nitriles
Mol File:189680-06-6.mol
2-Bromo-5-hydroxybenzonitrile Structure
2-Bromo-5-hydroxybenzonitrile Chemical Properties
Boiling point 321.2±32.0 °C(Predicted)
density 1.79±0.1 g/cm3(Predicted)
storage temp. Inert atmosphere,Room Temperature
pka8.01±0.18(Predicted)
form powder
color Brown
Safety Information
HS Code 2926907090
MSDS Information
2-Bromo-5-hydroxybenzonitrile Usage And Synthesis
Uses2-Bromo-5-hydroxybenzonitrile is a reagent used in the synthesis of various pharmaceutical goods.
Synthesis
3-Cyanophenol

873-62-1

2-BROMO-5-HYDROXYBENZONITRILE

189680-06-6

Step 1: Bromination reaction 3-Hydroxybenzonitrile (3.2 g, 26.8 mmol) was dissolved in glacial acetic acid (20 ml) and acetic acid solution (5 ml) of bromine (4.2 g, 23.3 mmol) was added slowly dropwise for a controlled period of 5 minutes. The reaction mixture was stirred at room temperature for 18 hours. After completion of the reaction, the mixture was filtered. The filtrate was poured into water (100 ml) containing a small amount of sodium thiosulfate to quench the unreacted bromine. The insoluble material was collected and the filter cake was mixed with warm methanol (15 ml) and filtered through diatomaceous earth. The filtrate was slowly diluted with water to precipitate, the precipitate was collected and dried to give 2-bromo-5-hydroxybenzonitrile in 22% yield (1.0 g) with a melting point of 183-185 °C.

References[1] ACS Medicinal Chemistry Letters, 2018, vol. 9, # 2, p. 120 - 124
[2] Patent: WO2011/34828, 2011, A1. Location in patent: Page/Page column 80
[3] Patent: WO2004/35556, 2004, A1. Location in patent: Page 95
2-Bromo-5-hydroxybenzonitrile Preparation Products And Raw materials
Raw materials3-Cyanophenol
Tag:2-Bromo-5-hydroxybenzonitrile(189680-06-6) Related Product Information
2-Bromo-5-ethoxy-4-hydroxy-benzonitrile 2-Bromo-4-(2-hydroxy-ethoxy)-5-methoxy-benzonitrile 2-Bromo-4-isopropoxy-5-methoxy-benzonitrile 2-Bromo-4-ethoxy-5-methoxy-benzonitrile 2-Bromo-4,5-dimethoxy-benzonitrile 2-BROMO-5-METHOXYBENZONITRILE 2-Bromo-4-hydroxy-5-methoxy-benzonitrile AKOS B005144 AKOS B005156 AKOS B004178 AKOS B005408 AKOS B005168 AKOS B004213 AKOS B005132 AKOS B005438 AKOS B005162 AKOS B005126 AKOS B005180