4-NITROPHENYLGLYOXAL HYDRATE

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Company Name: Shaanxi Dideu Medichem Co. Ltd
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Products Intro: Product Name:4-NITROPHENYLGLYOXAL HYDRATE
CAS:4996-22-9
Purity:95% Package:1KG;1USD|25KG;25USD|100KG;100USD
Company Name: Capot Chemical Co.,Ltd.
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Products Intro: Product Name:4-Nitrophenylglyoxal hydrate
CAS:4996-22-9
Purity:95%(Min,GC) Package:100g;1kg;5kg,10kg,25kg,50kg
Company Name: Alchem Pharmtech,Inc.
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Products Intro: Product Name:4-Nitrophenylglyoxal hydrate
CAS:4996-22-9
Purity:97+% Package:1g;10g;100g;;1kg Remarks:Z-00019
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Products Intro: Product Name:4-Nitrophenylglyoxal hydrate
CAS:4996-22-9
Purity:98% Min. Package:5KG;1KG
Company Name: Labnetwork lnc.
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Products Intro: Product Name:2,2-dihydroxy-1-(4-nitrophenyl)ethanone
CAS:4996-22-9
Purity:95% Package:100g; 1kg Remarks:LN00009981

4-NITROPHENYLGLYOXAL HYDRATE manufacturers

4-NITROPHENYLGLYOXAL HYDRATE Basic information
Product Name:4-NITROPHENYLGLYOXAL HYDRATE
Synonyms:2,2-dihydroxy-1-(4-nitrophenyl)ethanone;(4-Nitrophenyl)(oxo)acetaldehyde hydrate, 4-(Oxoacetyl)nitrobenzene hydrate;Ethanone, 2,2-dihydroxy-1-(4-nitrophenyl)-;4-NITROPHENYLGLYOXAL H2O;4-NITROPHENYLGLYOXAL HYDRATE;4-Nitrophenylglyoxal hydrate 95%;4-NITROPHENYLGLYOXAL HYDRATE, 95+%;2-(4-Nitrophenyl)-2-oxoacetaldehydehydrate
CAS:4996-22-9
MF:C8H7NO5
MW:197.14
EINECS:
Product Categories:
Mol File:4996-22-9.mol
4-NITROPHENYLGLYOXAL HYDRATE Structure
4-NITROPHENYLGLYOXAL HYDRATE Chemical Properties
Melting point 97-100 °C
Boiling point 356.7±27.0 °C(Predicted)
density 1.537±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
pka10.16±0.41(Predicted)
AppearanceOff-white to light yellow Solid
Safety Information
Hazard Codes Xi
Risk Statements 20/21/22-36/37/38
Safety Statements 26-36/37/39
Hazard Note Irritant
MSDS Information
4-NITROPHENYLGLYOXAL HYDRATE Usage And Synthesis
Synthesis
4-Nitroacetophenone

100-19-6

4-NITROPHENYLGLYOXAL HYDRATE

4996-22-9

GENERAL METHODS: A mixture of 4-nitroacetophenone (0.6 mmol) and ethylene bromide (0.06 mmol) in DMSO (1.1 mL) was placed in an open-top flask and heated in an oil bath (see Table 2 for specific temperatures and reaction times). After completion of the reaction (monitored by TLC), the reaction mixture was diluted with water (11 mL), salted with saturated NaCl solution and extracted with ethyl acetate (5 × 4 mL). Only in case of synthesis of arylglyoxal, the organic layer was additionally washed with aqueous Na2CO3 (0.12 mmol, dissolved in 2 mL of water), followed by saturated aqueous NaCl solution and dried with anhydrous Na2SO4. The extract was purified by column chromatography (eluent: petroleum ether/ethyl acetate gradient) to give pure 2,2-dihydroxy-1-(4-nitrophenyl)ethanone.

References[1] Tetrahedron Asymmetry, 2010, vol. 21, # 18, p. 2244 - 2248
[2] Tetrahedron, 2011, vol. 67, # 41, p. 8000 - 8008
[3] Journal of Fluorine Chemistry, 2010, vol. 131, # 12, p. 1289 - 1296
[4] Tetrahedron Letters, 2011, vol. 52, # 31, p. 4036 - 4038
[5] Tetrahedron, 2013, vol. 69, # 1, p. 22 - 28
4-NITROPHENYLGLYOXAL HYDRATE Preparation Products And Raw materials
Raw materials4-Nitroacetophenone
Tag:4-NITROPHENYLGLYOXAL HYDRATE(4996-22-9) Related Product Information
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