2-Hydroxy-1-(4-nitrophenyl)-1-ethanone

2-Hydroxy-1-(4-nitrophenyl)-1-ethanone Suppliers list
Company Name: Zhengzhou Guancheng Laboratory equipment Sales  Gold
Tel: 0371-88888888 qq272369594;2159423853qq
Email: 2723695949@qq.com
Company Name: J & K SCIENTIFIC LTD.  
Tel: 18210857532 18210857532
Email: jkinfo@jkchemical.com
Company Name: Wuhan Chemwish Technology Co., Ltd  
Tel: 86-027-67849912
Email: sales@chemwish.com
Company Name: Shanghai Jovan Biochemical Technology Co. Ltd.  
Tel: +86-021-61654350
Email: 1245958370@qq.com
Company Name: ChengDu TongChuangYuan Pharmaceutical Co.Ltd  
Tel: 028-83379370 13880556291
Email: tcy@tcypharm.com
2-Hydroxy-1-(4-nitrophenyl)-1-ethanone Basic information
Product Name:2-Hydroxy-1-(4-nitrophenyl)-1-ethanone
Synonyms:Ethanone, 2-hydroxy-1-(4-nitrophenyl)-;2-Hydroxy-1-(4-nitrophenyl)ethanone;2-Hydroxy-4'-nitroacetophenone;2-hydroxy-1-(4-nitrophenyl)ethan-1-one;2-Hydroxy-1-(4-nitrophenyl)-1-ethanone
CAS:64611-67-2
MF:C8H7NO4
MW:181.15
EINECS:
Product Categories:
Mol File:64611-67-2.mol
2-Hydroxy-1-(4-nitrophenyl)-1-ethanone Structure
2-Hydroxy-1-(4-nitrophenyl)-1-ethanone Chemical Properties
Melting point 140-143°C
Boiling point 338.4±17.0 °C(Predicted)
density 1.390±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
form solid
pka12.42±0.10(Predicted)
InChIInChI=1S/C8H7NO4/c10-5-8(11)6-1-3-7(4-2-6)9(12)13/h1-4,10H,5H2
InChIKeyDRGHCHSDUDQWHJ-UHFFFAOYSA-N
SMILESC(=O)(C1=CC=C([N+]([O-])=O)C=C1)CO
Safety Information
WGK Germany WGK 3
HazardClass IRRITANT
Storage Class11 - Combustible Solids
MSDS Information
2-Hydroxy-1-(4-nitrophenyl)-1-ethanone Usage And Synthesis
Synthesis
2-Bromo-4'-nitroacetophenone

99-81-0

2-HYDROXY-1-(4-NITROPHENYL)-1-ETHANONE

64611-67-2

Example 13A Synthesis of 2-hydroxy-1-(4-nitrophenyl)ethanone: 2-bromo-1-(4-nitrophenyl)ethanone (5 g, 20.5 mmol) and silver nitrate (5 g, 29.4 mmol) were dissolved in a solvent mixture of water (250 mL) and acetone (150 mL) and heated to reflux the reaction for 4 hours. After the reaction was completed, it was cooled to room temperature. The reaction mixture was filtered and the filtrate was extracted twice with dichloromethane. The organic phases were combined, dried with anhydrous sodium sulfate, filtered and concentrated. The concentrate was purified by silica gel fast column chromatography with 2:1 hexane/ethyl acetate as eluent to give 3.7 g (50% yield) of the target product 2-hydroxy-1-(4-nitrophenyl)ethanone. Thin layer chromatography (TLC) showed an Rf value of 0.4 (eluent ratio 1:1 hexane/ethyl acetate).

References[1] Advanced Synthesis and Catalysis, 2016, vol. 358, # 1, p. 74 - 80
[2] Journal of Organic Chemistry, 1989, vol. 54, # 18, p. 4473 - 4474
[3] European Journal of Medicinal Chemistry, 2013, vol. 67, p. 142 - 151
[4] Patent: US2003/225098, 2003, A1. Location in patent: Page 32
[5] Chemische Berichte, 1889, vol. 22, p. 203
2-Hydroxy-1-(4-nitrophenyl)-1-ethanone Preparation Products And Raw materials
Raw materials2-Bromo-4'-nitroacetophenone-->Water-->Silver nitrate-->Acetone
Tag:2-Hydroxy-1-(4-nitrophenyl)-1-ethanone(64611-67-2) Related Product Information
4-Nitrophenylglyoxylic acid ETHYL 4-NITROPHENYLGLYOXYLATE 2-Hydroxy-1-(4-nitrophenyl)-1-ethanone SALOR-INT L207462-1EA SALOR-INT L207349-1EA SALOR-INT L207446-1EA SALOR-INT L345571-1EA SALOR-INT L204277-1EA SALOR-INT L207136-1EA SALOR-INT L345504-1EA SALOR-INT L207535-1EA SALOR-INT L207527-1EA SALOR-INT L204218-1EA SALOR-INT L207268-1EA SALOR-INT L204374-1EA SALOR-INT L207187-1EA SALOR-INT L207063-1EA SALOR-INT L204307-1EA