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Manufacturers supply cost-effective and customizable 4-NITROTHIOANISOLE 701-57-5
- Molecular Formula: C7H7NO2S
- Molecular Weight: 169.204
- Appearance/Colour: Light yellow to brown solid
- Vapor Pressure: 0.00384mmHg at 25°C
- Melting Point: 66-69 °C(lit.)
- Refractive Index: 1.585 - 1.587
- Boiling Point: 289.4 °C at 760 mmHg
- Flash Point: 128.8 °C
- PSA: 71.12000
- Density: 1.27 g/cm3
- LogP: 2.83990
4-NITROTHIOANISOLE(Cas 701-57-5) Usage
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Synthesis Reference(s) |
Tetrahedron Letters, 24, p. 2575, 1983 DOI: 10.1016/S0040-4039(00)81985-1 |
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General Description |
4-Nitrothioanisole in acetone-d6 solution exhibits twofold barrier to rotation about the Csp2-S bond as 16.1±1.5kJ/mol. 4-Nitrothioanisole undergoes hydrogenation in the presence of sulfided Pd/C catalysts. |
InChI:InChI=1/C7H7NO2S/c1-11-7-4-2-6(3-5-7)8(9)10/h2-5H,1H3
701-57-5 Relevant articles
A protic ionic liquid, when entrapped in cationic reverse micelles, can be used as a suitable solvent for a bimolecular nucleophilic substitution reaction
Crosio, Matías A.,Correa, N. Mariano,Silber, Juana J.,Falcone, R. Darío
, p. 3170 - 3177 (2016)
In this work, we have explored how the c...
Evidence for the importance of polarizability in biomimetic catalysis involving cyclophane receptors
Ngola, Sarah M.,Dougherty, Dennis A.
, p. 4355 - 4360 (1996)
Cyclophanes 1-6 catalyze the nucleophili...
N-bromosuccinimide/HCl mediated reduction of sulfoxides to sulfides
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supporting information, p. 439 - 443 (2021/02/03)
An efficient reduction of sulfoxides to ...
Synthesis of Aryl Methyl Sulfides from Arysulfonyl Chlorides with Dimethyl Carbonate as the Solvent and C1 Source
Miao, Ren-Guan,Qi, Xinxin,Wu, Xiao-Feng
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A new procedure for the synthesis of ary...
Photoinduced Iron-Catalyzed ipso-Nitration of Aryl Halides via Single-Electron Transfer
Wu, Cunluo,Bian, Qilong,Ding, Tao,Tang, Mingming,Zhang, Wenkai,Xu, Yuanqing,Liu, Baoying,Xu, Hao,Li, Hai-Bei,Fu, Hua
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A photoinduced iron-catalyzed ipso-nitra...
t-BuOK-promoted methylthiolation of aryl fluorides with dimethyldisulfide under transition-metal-free and mild conditions
Huang, Dayun,Wu, Xiangmei
, (2021/03/24)
In the presence of potassium tert-butoxi...
701-57-5 Process route
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71-23-8
propan-1-ol
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29843-53-6
dimethyl(p-nitrophenyl)sulfonium perchlorate
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-
100-02-7,78813-13-5,89830-32-0
4-nitro-phenol
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-
701-57-5
1-methylthio-4-nitro-benzene
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7244-77-1
1-nitro-4-propoxybenzene
| Conditions | Yield |
|---|---|
|
With
sodium hydroxide;
at 80 ℃;
|
22.8%
|
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With
sodium hydroxide;
at 80 ℃;
Rate constant;
Product distribution;
Kinetics;
various temperature and pH (11.61 - 11.21);
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937-32-6
4-nitrobenzenesulfenyl chloride
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-
594-27-4
tetramethylstannane
-
-
701-57-5
1-methylthio-4-nitro-benzene
-
-
100-32-3
di(p-nitrophenyl) disulfide
| Conditions | Yield |
|---|---|
|
tetrakis(triphenylphosphine) palladium(0);
In
tetrahydrofuran;
at 25 ℃;
for 4h;
Yields of byproduct given;
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701-57-5 Upstream products
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13118-32-6
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701-57-5 Downstream products
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940-12-5
p-nitrophenyl methyl sulfoxide
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2976-30-9
1-methanesulfonyl-4-nitrobenzene
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7205-88-1
1-[(chloromethyl)sulfanyl]-4-nitrobenzene
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713-66-6
4-nitrophenyl trichloromethylsulfide