Basic information Safety Supplier Related

METHYL M-NITROPHENYL CARBINOL

Basic information Safety Supplier Related

METHYL M-NITROPHENYL CARBINOL Basic information

Product Name:
METHYL M-NITROPHENYL CARBINOL
Synonyms:
  • METHYL M-NITROPHENYL CARBINOL
  • 3-NITROPHENYLMETHYLCARBINOL
  • 1-(3-NITROPHENYL)ETHANOL
  • 1-(3-NIitrophenyl)ethanol
  • 2-methyl-3-nitroBenzenemethanol
  • 1-(3-Nitrophenyl)ethan-1-ol
  • Benzenemethanol, α-methyl-3-nitro-
  • Benzenemethanol, a-methyl-3-nitro-
CAS:
5400-78-2
MF:
C8H9NO3
MW:
167.16
Product Categories:
  • Benzhydrols, Benzyl & Special Alcohols
Mol File:
5400-78-2.mol
More
Less

METHYL M-NITROPHENYL CARBINOL Chemical Properties

Melting point:
62.5 °C
Boiling point:
154-155 °C(Press: 9 Torr)
Density 
1.2049 g/cm3(Temp: 31 °C)
storage temp. 
Sealed in dry,Room Temperature
pka
13.89±0.20(Predicted)
Appearance
Off-white to light yellow Solid
More
Less

Safety Information

RTECS 
DJ3100438
HS Code 
2906290090
More
Less

METHYL M-NITROPHENYL CARBINOL Usage And Synthesis

Synthesis

121-89-1

5400-78-2

1. Sodium borohydride (NaBH4, 2.20 g, 58.1 mmol) was slowly added to a solution of methanol (MeOH, 100 mL) containing 1-(3-nitrophenyl)ethanone (ID29, 2.32 g, 14.0 mmol) at 0°C. 2. The reaction mixture was stirred continuously at 0 °C for 1 hour. 3. After completion of the reaction, most of the methanol was removed by concentration under reduced pressure. 4. 4. The residue was diluted with ethyl acetate (EtOAc, 150 mL) and water (50 mL) and the organic layer was separated. 5. The organic layer was washed sequentially with water (50 mL) and saturated saline (50 mL) and then dried over anhydrous sodium sulfate (Na2SO4). 6. The desiccant was removed by filtration, and the filtrate was concentrated under reduced pressure to obtain the crude product. 7. The crude product was dried under vacuum to afford 1-(3-nitrophenyl)ethanol (ID30) as a pale yellow oil (2.23 g, 95% yield). 8. The structure of the product was determined by 1H NMR. 8. The structure of the product was confirmed by 1H NMR (CDCl3, 600 MHz): δ 8.25 (s, 1H), 8.12 (ddd, J = 8.4, 1.2, 1.2 Hz, 1H), 7.72 (d, J = 7.2 Hz, 1H), 7.52 (dd, J = 8.1, 8.1 Hz, 1H), 5.02 (q, J = 6.6 Hz, 1H), 2.07 (s, J = 6.6 Hz, 1H), 5.02 (q, J = 6.6 Hz, 1H), 5.02 (q, J = 6.6 Hz, 1H), 2.02 (q, J = 6.6 Hz, 1H), 2.07 (s), 2.07 (s), 1H). ), 2.07 (s, 1H), 1.54 (d, J = 6.6 Hz, 3H).

References

[1] Green Chemistry, 2018, vol. 20, # 9, p. 2118 - 2124
[2] Journal of the Iranian Chemical Society, 2015, vol. 12, # 7, p. 1221 - 1226
[3] Synthetic Communications, 1990, vol. 20, # 6, p. 849 - 854
[4] Chemistry Letters, 1987, p. 181 - 184
[5] Synthesis, 2009, # 23, p. 4058 - 4062

METHYL M-NITROPHENYL CARBINOLSupplier

Jiangsu Aikon Biopharmaceutical R&D co.,Ltd.
Tel
025-66113011 17798518460
Email
cfzhang@aikonchem.com
Bide Pharmatech Ltd.
Tel
400-164-7117 13681763483
Email
product02@bidepharm.com
Xinyanhe Pharmatech Co.,Ltd
Tel
0519-85252752 15366845260
Email
taihuaren@vip.163.com
Zhengzhou Guancheng Laboratory equipment Sales
Tel
0371-88888888 272369594
Email
2723695949@qq.com
Shanghai YuanYe Biotechnology Co., Ltd.
Tel
021-61312847; 18021002903
Email
3008007409@qq.com