37629-51-9

  • Product Name:1-(4-METHOXYPHENYL)-2-NITROPROPENE
  • Molecular Formula:C10H11NO3
  • Purity:99%
  • Molecular Weight:193.202
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Product Details;

CasNo: 37629-51-9

Molecular Formula: C10H11NO3

Quality Manufacturer Supply 99% Pure 1-(4-METHOXYPHENYL)-2-NITROPROPENE 37629-51-9 Low Price

  • Molecular Formula:C10H11NO3
  • Molecular Weight:193.202
  • Vapor Pressure:0.000551mmHg at 25°C 
  • Boiling Point:321.7oC at 760 mmHg 
  • Flash Point:147.4oC 
  • PSA:55.05000 
  • Density:1.156g/cm3 
  • LogP:2.85590 

1-(4-METHOXYPHENYL)-2-NITROPROPENE(Cas 37629-51-9) Usage

1-(4-methoxyphenyl)-2-nitropropene is non-planar. These chemicals, including 1-(4-methoxyphenyl)-2-nitropropene, are utilized in various applications, ranging from organic synthesis to the pharmaceutical industry.

InChI:InChI=1/C10H11NO3/c1-8(11(12)13)7-9-3-5-10(14-2)6-4-9/h3-7H,1-2H3/b8-7+

37629-51-9 Relevant articles

Discovery of Cytochrome P450 4F11 Activated Inhibitors of Stearoyl Coenzyme A Desaturase

Winterton, Sarah E.,Capota, Emanuela,Wang, Xiaoyu,Chen, Hong,Mallipeddi, Prema L.,Williams, Noelle S.,Posner, Bruce A.,Nijhawan, Deepak,Ready, Joseph M.

, p. 5199 - 5221 (2018/06/13)

Stearoyl-CoA desaturase (SCD) catalyzes ...

Catalyst- and Substituent-Controlled Switching of Chemoselectivity for the Enantioselective Synthesis of Fully Substituted Cyclobutane Derivatives via 2 + 2 Annulation of Vinylogous Ketone Enolates and Nitroalkene

Akula, Pavan Sudheer,Hong, Bor-Cherng,Lee, Gene-Hsiang

supporting information, p. 7835 - 7839 (2019/01/04)

The first regioselective, diastereoselec...

Catalytic asymmetric Tamura cycloadditions involving nitroalkenes

Manoni, Francesco,Farid, Umar,Trujillo, Cristina,Connon, Stephen J.

, p. 1463 - 1474 (2017/02/15)

The first examples of asymmetric Tamura ...

37629-51-9 Process route

Nitroethane
79-24-3

Nitroethane

4-methoxy-benzaldehyde
123-11-5

4-methoxy-benzaldehyde

1-methoxy-4-((E)-2-nitroprop-1-enyl)benzene
37629-51-9

1-methoxy-4-((E)-2-nitroprop-1-enyl)benzene

Conditions
Conditions Yield
With ammonium acetate; In toluene; at 100 ℃; for 22h;
99%
MCM-41-NH2; at 90 ℃; for 6h;
95%
With piperidine; iron(III) chloride; In toluene; for 6h; Reflux;
94%
aminopropyl-functionalized silica; at 110 ℃; for 5h;
92%
With phenolformaldehyde-based ethylenediamine-modified polymer; at 90 ℃; for 6h;
84%
With ammonium acetate; for 0.583333h; Heating;
81%
With O-(tert-butyldiphenylsilyl)-L-tyrosine lithium salt; magnesium sulfate; In dichloromethane; at 25 ℃; for 96h; stereoselective reaction;
81%
With isobutylamine; In acetic acid; at 50 ℃; for 3h; under 7500600 Torr;
80%
morpholine on silica gel; In acetonitrile; at 25 ℃; for 0.1h;
78%
With ammonium acetate; at 60 ℃; for 4h;
76%
With ammonium acetate; at 120 - 130 ℃; for 2h;
73%
With ammonium acetate; for 2h; Heating;
71%
With N-butylamine; In toluene; for 8h; Reflux;
66%
With CsNaX zeolite; for 24h; Heating;
65%
Nitroethane; 4-methoxy-benzaldehyde; With potassium tert-butylate; In tetrahydrofuran; tert-butyl alcohol; at 0 - 20 ℃; for 12h; Inert atmosphere;
With trifluoroacetic anhydride; In dichloromethane; at -10 ℃; for 0.5h; Inert atmosphere;
With triethylamine; In dichloromethane; at -10 ℃; for 0.5h; Inert atmosphere;
65%
With ammonium acetate; at 110 ℃; for 45h; Inert atmosphere;
49.5%
With ammonium acetate; Heating;
48%
With n-Pentylamine; at 20 ℃;
 
With ethanol; N-butylamine;
 
With ammonium acetate; acetic acid;
 
 
 
With propylamine; Ambient temperature;
 
 
 
With ammonium acetate; for 2h; Inert atmosphere; Reflux;
 
With acetic acid; N-butylamine; at 60 ℃; Sonication;
 
2-nitro-1-hydroxy-1-(4-methoxy-phenyl)-propane
148527-33-7

2-nitro-1-hydroxy-1-(4-methoxy-phenyl)-propane

1-methoxy-4-((E)-2-nitroprop-1-enyl)benzene
37629-51-9

1-methoxy-4-((E)-2-nitroprop-1-enyl)benzene

Conditions
Conditions Yield
With triethylamine; triphenylphosphine; In tetrachloromethane; for 2h; Heating;
95%
Multi-step reaction with 2 steps
1: CH2Cl2
2: NEt3 / CH2Cl2
With triethylamine; In dichloromethane;
 
Multi-step reaction with 2 steps
1: pyridine / 2 h / Ambient temperature
2: sodium carbonate / benzene / 5 h / Heating
With pyridine; sodium carbonate; In benzene;
 
With 1H-imidazole; iodine; In dichloromethane; for 0.833333h; Reagent/catalyst;
 

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