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1-(2-nitrophenyl)ethanol

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1-(2-nitrophenyl)ethanol manufacturers

1-(2-nitrophenyl)ethanol Basic information
Product Name:1-(2-nitrophenyl)ethanol
Synonyms:1-(2-Nitrophenyl)ethyl Alcohol;α-Methyl-2-nitro-benzeneMethanol;α-Methyl-2-nitrobenzyl Alcohol;alpha-(2-Nitrophenyl)ethanol;alpha-Methyl-2-nitrobenzyl alcohol;NSC 47195;2-methyl-2-nitroBenzenemethanol;1-(2-Nitrophenyl)
CAS:3205-25-2
MF:C8H9NO3
MW:167.16
EINECS:
Product Categories:Aromatics;Miscellaneous Reagents
Mol File:3205-25-2.mol
1-(2-nitrophenyl)ethanol Structure
1-(2-nitrophenyl)ethanol Chemical Properties
Melting point 40-41℃
Boiling point 106-107°C 1mmHg.
density 1.2300 g/cm3 (20 ºC)
refractive index 1.5572 (589.3 nm 20℃)
storage temp. Sealed in dry,Room Temperature
solubility Dichloromethane, Ether, Ethyl Acetate, Methanol
form Solid
pka13.84±0.20(Predicted)
color Pale Yellow
InChIInChI=1S/C8H9NO3/c1-6(10)7-4-2-3-5-8(7)9(11)12/h2-6,10H,1H3
InChIKeyDSDBYQDNNWCLHL-UHFFFAOYSA-N
SMILESC(C1C=CC=CC=1N(=O)=O)(O)C
CAS DataBase Reference3205-25-2
Safety Information
HS Code 2906290090
MSDS Information
1-(2-nitrophenyl)ethanol Usage And Synthesis
Chemical PropertiesYellow Oil
Uses(R,S)-1-(2-Nitrophenyl)ethanol (cas# 3205-25-2) is a compound useful in organic synthesis.
Synthesis
2-Nitroacetophenone

577-59-3

(S)-1-(2-nitrophenyl)ethanol

80379-10-8

General procedure for the synthesis of (S)-1-(2-nitrophenyl)ethan-1-ol from o-nitroacetophenone: Synthesis of (RS)-1-(2-nitrophenyl)ethan-1-ol: Sodium borohydride (0.69 g, 18.16 mmol) was added in small portions to a mixed solution of 2-nitroacetophenone (1.0 g, 6.06 mmol) dissolved in methanol (9 mL) and 1,4-dioxane (6 mL) (cf. Dong et al., 2005). The reaction mixture was stirred at room temperature for 30 min and then concentrated under vacuum. The residue was diluted with ethyl acetate (50 mL) and washed sequentially with water (10 mL) and brine (10 mL). The organic phase was dried over anhydrous sodium sulfate and concentrated in vacuum to give racemic (RS)-1-(2-nitrophenyl)ethanol (1.02 g, 100% yield). 1H NMR (400 MHz, CDCl3) data: δ 7.90 (m, 1H, Ph-H), 7.84 (m, 1H, Ph-H), 7.66 (m, 1H, Ph-H), 7.44 (m, 1H, Ph-H), 5.42 (m, 1H, Ph-CH), 2.33 (d, 1H, J = 3.5 Hz, OH), 1.58 (d, 3H, J = 5.1 Hz, CH3).

References[1] Patent: US9200319, 2015, B2. Location in patent: Page/Page column 57
[2] Journal of Organometallic Chemistry, 2016, vol. 808, p. 68 - 77
[3] Chemistry - A European Journal, 2012, vol. 18, # 31, p. 9628 - 9637
[4] Applied Organometallic Chemistry, 2018, vol. 32, # 3,
[5] Organic Letters, 2018, vol. 20, # 11, p. 3403 - 3407
1-(2-nitrophenyl)ethanol Preparation Products And Raw materials
Raw materials2-Nitroacetophenone-->2-Nitrotoluene-->2-Ethylnitrobenzene-->N,N-Dimethylformamide-->Sodium borohydride-->1,4-Dioxane-->Methanol
Tag:1-(2-nitrophenyl)ethanol(3205-25-2) Related Product Information
1-(2-Nitrophenyl)-1,2-ethanediol CAGED ATP, DISODIUM SALT NITR 5/AM 'CAGED GTP Adenosine 3',5'-cyclic monophosphate, P1-(2-nitrophenyl)ethyl ester [3-(2-Nitrophenyl)oxiran-2-yl](phenyl)methanone Nitr 5 tetrasodium salt CAGED CGMP nitr 5 nitr 2 CAGED INS(1,4,5)P3, TRISODIUM SALT nitr 7 4-Bromo A-23187, 1-(4,5-dimethoxy-2-nitrophenyl)ethyl ester 1-(2-Nitrophenyl)ethyl phosphate, diammonium salt Caged glutamic acid Hydroxy(2-nitrophenyl)acetonitrile Caged aspartic acid, sodium salt 1-(alpha-Glycerophosphoryl)-D-myo-inositol 4,5-bisphosphate, P4(5)-1-(2-nitrophenyl)ethyl ester, 3Na