29816-55-5
- Product Name:1-(4-Methylphenyl)-2-nitropropene
- Molecular Formula:C10H11NO2
- Purity:99%
- Molecular Weight:177.203
Product Details;
CasNo: 29816-55-5
Molecular Formula: C10H11NO2
Quality Factory Supply Top Purity 1-(4-Methylphenyl)-2-nitropropene 29816-55-5 On Stock
- Molecular Formula:C10H11NO2
- Molecular Weight:177.203
- Vapor Pressure:0.00563mmHg at 25°C
- Melting Point:55 °C
- Refractive Index:1.577
- Boiling Point:282.7 °C at 760 mmHg
- Flash Point:123.9 °C
- PSA:45.82000
- Density:1.112 g/cm3
- LogP:3.15570
1-(4-Methylphenyl)-2-nitropropene(Cas 29816-55-5) Usage
Chemical Properties |
Pale yellow crystalline powder |
Description | 1-(4-Methylphenyl)-2-nitropropene, also known by synonyms such as p-Methyl-β-nitrostyrene and 2-nitro-1-p-tolyl-propene, is an organic compound commonly used as a precursor in organic synthesis. |
Uses | 1-(4-Methylphenyl)-2-nitropropene is likely employed as a starting material or intermediate in the synthesis of various organic compounds. Its applications may extend to chemical reactions in the pharmaceutical, industrial, and research sectors. Researchers and chemists should exercise caution and comply with safety guidelines and legal requirements when working with such compounds. |
InChI:InChI=1/C10H11NO2/c1-8-3-5-10(6-4-8)7-9(2)11(12)13/h3-7H,1-2H3/b9-7+
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supporting information, p. 13721 - 13724 (2019/09/16)
Pd-Catalyzed sequential reactions to aff...
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29816-55-5 Process route
- 79-24-3
Nitroethane
- 104-87-0
4-methyl-benzaldehyde
- 52287-56-6,29816-55-5
1-(p-tolyl)-2-nitropropene
Conditions | Yield |
---|---|
With ammonium acetate; at 110 ℃; for 16h;
|
100% |
With (2-hydroxyethyl)ammonium formate; at 20 ℃; for 4.1h; Ionic liquid;
|
95% |
With ammonium acetate; at 120 ℃; for 2h;
|
95% |
With ammonium acetate; Reflux;
|
79% |
With piperidine; for 0.116667h; Irradiation;
|
55% |
With n-Pentylamine;
|
|
With ethylamine; In ethanol;
|
|
With methylamine hydrochloride; potassium acetate; trimethyl orthoformate; In methanol; Heating;
|
|
With acetic acid; N-butylamine; for 1h; Heating;
|
|
With ammonium acetate;
|
|
With (2-hydroxyethyl)ammonium formate; at 20 ℃; Inert atmosphere;
|
|
With ammonium acetate; In acetic acid; for 1 - 2h; Reflux;
|
- 79-24-3
Nitroethane
- 104-84-7
para-methylbenzylamine
- 52287-56-6,29816-55-5
1-(p-tolyl)-2-nitropropene
Conditions | Yield |
---|---|
With 4-(4-fluorophenyl)naphthalene-1,2-dione; oxygen; at 80 ℃; for 12h;
|
71% |
29816-55-5 Upstream products
-
79-24-3
Nitroethane
-
104-87-0
4-methyl-benzaldehyde
-
135711-44-3
Butyl-(2-nitro-1-p-tolyl-propyl)-amine
-
53982-05-1
2-nitro-1-(p-tolyl)propan-1-ol
29816-55-5 Downstream products
-
64-11-9
4-methylamphetamine
-
2096-86-8
p-Tolylaceton
-
29865-50-7
1-(4'-methylphenyl)-2-nitropropane
-
1723-25-7
ethyl 2,3-dioxobutyrate
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